Recent Advances in Synthesis of Non-Alternating Polyketone Generated by Copolymerization of Carbon Monoxide and Ethylene

The copolymers of carbon monoxide (CO) and ethylene, namely aliphatic polyketones (PKs), have attracted considerable attention due to their unique property and degradation. Based on the arrangement of the ethylene and carbonyl groups in the polymer chain, PKs can be divided into perfect alternating and non-perfect alternating copolymers. Perfect alternating PKs have been previously reviewed, we herein focus on recent advances in the synthesis of PKs without a perfect alternating structure including non-perfect alternating PKs and PE with in-chain ketones. The chain structure of PKs, catalytic copolymerization mechanism, and non-alternating polymerization catalysts including phosphine–sulfonate Pd, diphosphazane monoxide (PNPO) Pd/Ni, and phosphinophenolate Ni catalysts are comprehensively summarized. This review aims to enlighten the design of ethylene/CO non-alternating polymerization catalysts for the development of new polyketone materials.

The first example of the metal-catalyzed synthesis of PKs was reported in 1951, in which CO/ethylene copolymerization was catalyzed by K 2 Ni[CN] 4 to produce low-melting oligomers [38].In the subsequent decades, various nickel and palladium catalysts have The first example of the metal-catalyzed synthesis of PKs was reported in 1951, in which CO/ethylene copolymerization was catalyzed by K2Ni[CN]4 to produce low-melting oligomers [38].In the subsequent decades, various nickel and palladium catalysts have been developed for alternating copolymerizing ethylene and CO to synthesize aliphatic PKs [39][40][41][42][43][44][45][46][47].A breakthrough is the diphosphine palladium catalysts discovered by Drent in 1991, which are highly efficient for alkene/CO copolymerization [48].In 1996, a CO/ethylene/propylene terpolymer called "Carilon" was successfully commercialized by Shell company, but production of "Carilon" was closed in 2000 due to strategic changes [2].Hyosung company began to produce the same PKs in 2013, and the current annual production of PKs has reached 50,000 tons [49].These engineering plastics are commercially available for food contact, industry, and medical equipment.
Because the insertion of CO into the five-membered Pd-acyl-chelates is kinetically favored over ethylene insertion and successive insertion of CO is thermodynamically prohibited, perfect alternating PKs are often produced by Ni/Pd catalyzed copolymerization of ethylene and CO.In the early period, perfect alternating PKs received considerable attention in both academic and industrial fields (Figure 1).Recently, PKs without a perfect alternating structure, including non-perfect alternating PKs and polyethylene (PE) with in-chain ketones, have also attracted increasing interest (Figure 1).In 2002, non-alternating CO/ethylene copolymerization was first realized using phosphine-sulfonate Pd catalysts developed by Drent [50].With improved flexibility, non-alternating PKs have potential applications in many industrial fields such as textile fibers and packing films.PE with inchain ketones was recently developed and exhibited similar mechanical properties to commercial high-density polyethylene (HDPE) and better degradability and hydrophily [51,52].Introducing a small amount of CO in polyolefins provides a promising strategy to balance the demand for polyolefins and expectations of environmental friendliness, and PE with in-chain ketones can be understood as degradable HDPE.references [47,48]; (B): reference [50]; (C): reference [51].
Perfect alternating PKs have been systematically summarized in previous reviews [1,[3][4][5][53][54][55][56][57].In this review covering the literature published until the end of 2023, we focus on recent advances in the synthesis of PKs without a perfect alternating structure including non-perfect alternating PKs and PE with in-chain ketones.The chain structure of PKs without a perfect alternating structure, catalytic copolymerization mechanism, and Ni/Pd catalysts are summarized.Based on the arrangement of the ethylene and carbonyl groups, the structural fragments and corresponding NMR shifts of PKs without a perfect alternating structure are classified in Table 2.  Alternating PKs in mixture of hexafluoroisopropanol (HFIP, 90%) and C6D6 (10%), reference [48].b PE with in-chain ketones from 13 CO/ethylene copolymerization, in C2D2Cl4, 383K, reference [51].c Non-perfect alternating PKs in HFIP, reference [58].
Carbonyl content and extra ethylene (C2) insertion are the two most important structural parameters of PKs, defined as total mol % CO units relative to all monomer units [59] and total mol % ethylene of copolymer involved in non-alternation [50], respectively.Carbonyl content can be calculated by 1 H NMR according to the formula reported by Sen [59]: Based on the arrangement of the ethylene and carbonyl groups, the structural fragments and corresponding NMR shifts of PKs without a perfect alternating structure are classified in Table 2.

Chain Structure of PKs without a Perfect Alternating Structure
PKs without a perfect alternating structure have sequential ethylene units in a polymer chain, which originates from sequential ethylene insertion during the copolymerization of ethylene and CO.The resulting microstructure and melting temperatures (Tm) of three kinds of PKs are shown in Table 1.Based on the arrangement of the ethylene and carbonyl groups, the structural fragments and corresponding NMR shifts of PKs without a perfect alternating structure are classified in Table 2.  Alternating PKs in mixture of hexafluoroisopropanol (HFIP, 90%) and C6D6 (10%), reference [48].b PE with in-chain ketones from 13 CO/ethylene copolymerization, in C2D2Cl4, 383K, reference [51].c Non-perfect alternating PKs in HFIP, reference [58].
Carbonyl content and extra ethylene (C2) insertion are the two most important structural parameters of PKs, defined as total mol % CO units relative to all monomer units [59] and total mol % ethylene of copolymer involved in non-alternation [50], respectively.Carbonyl content can be calculated by 1 H NMR according to the formula reported by Sen [59]: I2, I4, I5, I7, I8, I9, I11, I12, and I13 are the integral of 1 H NMR signal of corresponding methylene.

Chain Structure of PKs without a Perfect Alternating Structure
PKs without a perfect alternating structure have sequential ethylene units in a polymer chain, which originates from sequential ethylene insertion during the copolymerization of ethylene and CO.The resulting microstructure and melting temperatures (Tm) of three kinds of PKs are shown in Table 1.Based on the arrangement of the ethylene and carbonyl groups, the structural fragments and corresponding NMR shifts of PKs without a perfect alternating structure are classified in Table 2.  Alternating PKs in mixture of hexafluoroisopropanol (HFIP, 90%) and C6D6 (10%), reference [48].b PE with in-chain ketones from 13 CO/ethylene copolymerization, in C2D2Cl4, 383K, reference [51].c Non-perfect alternating PKs in HFIP, reference [58].
Carbonyl content and extra ethylene (C2) insertion are the two most important structural parameters of PKs, defined as total mol % CO units relative to all monomer units [59] and total mol % ethylene of copolymer involved in non-alternation [50], respectively.Carbonyl content can be calculated by 1 H NMR according to the formula reported by Sen [59]: I2, I4, I5, I7, I8, I9, I11, I12, and I13 are the integral of 1 H NMR signal of corresponding methylene.including non-perfect alternating PKs and PE with in-chain ketones.The chain structure of PKs without a perfect alternating structure, catalytic copolymerization mechanism, and Ni/Pd catalysts are summarized.

Chain Structure of PKs without a Perfect Alternating Structure
PKs without a perfect alternating structure have sequential ethylene units in a polymer chain, which originates from sequential ethylene insertion during the copolymerization of ethylene and CO.The resulting microstructure and melting temperatures (Tm) of three kinds of PKs are shown in Table 1.Based on the arrangement of the ethylene and carbonyl groups, the structural fragments and corresponding NMR shifts of PKs without a perfect alternating structure are classified in Table 2. 23.8 b a Alternating PKs in mixture of hexafluoroisopropanol (HFIP, 90%) and C6D6 (10%), reference [48].b PE with in-chain ketones from 13 CO/ethylene copolymerization, in C2D2Cl4, 383K, reference [51].c Non-perfect alternating PKs in HFIP, reference [58].
Carbonyl content and extra ethylene (C2) insertion are the two most important structural parameters of PKs, defined as total mol % CO units relative to all monomer units [59] and total mol % ethylene of copolymer involved in non-alternation [50], respectively.Carbonyl content can be calculated by 1 H NMR according to the formula reported by Sen [59]: I2, I4, I5, I7, I8, I9, I11, I12, and I13 are the integral of 1 H NMR signal of corresponding methylene.including non-perfect alternating PKs and PE with in-chain ketones.The chain structure of PKs without a perfect alternating structure, catalytic copolymerization mechanism, and Ni/Pd catalysts are summarized.

Chain Structure of PKs without a Perfect Alternating Structure
PKs without a perfect alternating structure have sequential ethylene units in a polymer chain, which originates from sequential ethylene insertion during the copolymerization of ethylene and CO.The resulting microstructure and melting temperatures (Tm) of three kinds of PKs are shown in Table 1.Based on the arrangement of the ethylene and carbonyl groups, the structural fragments and corresponding NMR shifts of PKs without a perfect alternating structure are classified in Table 2. 23.8 b a Alternating PKs in mixture of hexafluoroisopropanol (HFIP, 90%) and C6D6 (10%), reference [48].b PE with in-chain ketones from 13 CO/ethylene copolymerization, in C2D2Cl4, 383K, reference [51].c Non-perfect alternating PKs in HFIP, reference [58].
Carbonyl content and extra ethylene (C2) insertion are the two most important structural parameters of PKs, defined as total mol % CO units relative to all monomer units [59] and total mol % ethylene of copolymer involved in non-alternation [50], respectively.Carbonyl content can be calculated by 1 H NMR according to the formula reported by Sen [59]: I2, I4, I5, I7, I8, I9, I11, I12, and I13 are the integral of 1 H NMR signal of corresponding methylene.including non-perfect alternating PKs and PE with in-chain ketones.The chain structure of PKs without a perfect alternating structure, catalytic copolymerization mechanism, and Ni/Pd catalysts are summarized.

Chain Structure of PKs without a Perfect Alternating Structure
PKs without a perfect alternating structure have sequential ethylene units in a polymer chain, which originates from sequential ethylene insertion during the copolymerization of ethylene and CO.The resulting microstructure and melting temperatures (Tm) of three kinds of PKs are shown in Table 1.Based on the arrangement of the ethylene and carbonyl groups, the structural fragments and corresponding NMR shifts of PKs without a perfect alternating structure are classified in Table 2. 23.8 b a Alternating PKs in mixture of hexafluoroisopropanol (HFIP, 90%) and C6D6 (10%), reference [48].b PE with in-chain ketones from 13 CO/ethylene copolymerization, in C2D2Cl4, 383K, reference [51].c Non-perfect alternating PKs in HFIP, reference [58].
Carbonyl content and extra ethylene (C2) insertion are the two most important structural parameters of PKs, defined as total mol % CO units relative to all monomer units [59] and total mol % ethylene of copolymer involved in non-alternation [50], respectively.Carbonyl content can be calculated by 1 H NMR according to the formula reported by Sen [59]: I2, I4, I5, I7, I8, I9, I11, I12, and I13 are the integral of 1 H NMR signal of corresponding methylene.Carbonyl content and extra ethylene (C2) insertion are the two most important structural parameters of PKs, defined as total mol % CO units relative to all monomer units [59] and total mol % ethylene of copolymer involved in non-alternation [50], respectively.Carbonyl content can be calculated by 1  Extra ethylene (C2) insertion can be calculated by 13 C NMR (signal of methylene) according to the formula reported by Chen [58]: I 2 , I 4 , I 7 , and I 11 are the integral of 13 C NMR signal of corresponding methylene.
In the case of PE with in-chain ketones, in addition to carbonyl content, the proportion of different carbonyl groups (1, 3, 6, and 14) in PKs also becomes important because the carbonyl content is too low to display obvious differences [51,52,[60][61][62].The 13 C NMR signals of different carbonyl groups (1, 3, 6, and 14) and adjacent methylene (2, 4, 7, and 15) almost relatively isolate each other; therefore, the proportion of each kind of carbonyl can be calculated.Due to the low carbonyl content, the replacement of 13 CO stock is used to enhance the sensitivity of the characteristic carbonyl [51,52].Owing to the unique and intense signal of carbonyl, IR spectroscopy provides another practical measurement of the carbonyl content of PE with in-chain ketones, and a series of PKs with known carbonyl contents is need to draw a standard curve [52,63,64].
The relationship between the properties and microstructure of the copolymer has been systematically studied by Müller and Mecking [65,66].Properties of PKs without a perfect alternating structure, such as T m , thermal decomposition temperature, and melt viscosity, for the microstructure, have a strong dependence on the copolymer, the CO content, and molecular weight, and the concentration of methyl branches along the chain directly determines the properties of the copolymer.In general, the properties of the copolymer are close to that of PE when the carbonyl content is low.
When the carbonyl content is high (>35%), the T m of the copolymer decreases with the decrease of the carbonyl content because the multiple ethylene insertion destroys the dipolar interaction between the carbonyl groups in the alternating structure [50,[67][68][69].However, at a low carbonyl content (<30%), the properties of the copolymer are close to PE, and the decrease in carbonyl content usually leads to an increase in crystallinity, so the T m of the copolymer decreases with the decrease in carbonyl content [59].

Catalytic Copolymerization Mechanism
Successive CO insertion is thermodynamically prohibited in CO/ethylene copolymerization [56].Therefore, the key to obtain alternating or non-alternating copolymers is whether the ethylene sequential insertion with unfavorable kinetics can be achieved by the improvement of the catalyst system and the availability of copolymerization conditions.
Phosphine-sulfonate ligand palladium catalyst systems achieved the first example of non-alternating copolymerization of CO and ethylene, of which the catalytic mechanisms have been investigated scientifically [59,[70][71][72].Therefore, take the example of typical bidentate [P, P] palladium complexes (alternating copolymerization catalysts) and neutral phosphine-sulfonate ligated Pd complexes (Scheme 1), the origins of sequential insertions of ethylene are proved to be (1) destabilization of Pd-acyl β-chelates A (phosphine-sulfonate); (2) facile decarbonylation of six-membered Pd-acyl chelates D [67,68,70].As shown in Scheme 1, five-membered Pd-acyl β-chelates A existing in CO/ethylene copolymerization catalyzed by bidentate [P, P] and phosphine-sulfonate palladium complexes, can accept insertions from ethylene or CO [67].The stability of β-chelates A is lower in the case of phosphine-sulfonate ligands; therefore, the chelate cycle is easily opened by ethylene [68,71].The binding affinities of CO and ethylene to β-chelates A have been measured by Sen in 2009 [59].Although the ratio of binding affinities determined credibly by NMR seems reliable enough to explain the multiple insertions of ethylene, Sen believes decarbonylation also plays a crucial part in the non-alternation [59].Thus, the second reason involving decarbonylation of six-membered Pd-acyl chelates D can be considered as a supplement to the first reason, which together constitute the reasons for the non-alternating copolymerization ability of neutral phosphine-sulfonate ligated palladium complexes.
The relatively facile decarbonylation is also related to the instability of the corresponding Pd-acyl chelates D of phosphine-sulfonate ligands [59,71].Although the destabilization of Pd-acyl -chelates and decarbonylation could partly explain why non-alternating copolymerization occurs, most mechanisms cannot escape the scope of phenomenological theory.In fact, it is extremely difficult to find a direct connection between the ability of non-alternating copolymerization and the structure of ligands or catalysts.Therefore, there is still no perfect theory to predict new catalyst systems that can achieve non-alternating copolymerization of CO and ethylene.
However, some researchers have made outstanding contributions to exploring the nature of the origin of non-alternating copolymerization [72][73][74][75][76].In different unique polymerizations realized by phosphine sulfonate palladium catalysts, similar cis/trans isomerization (Scheme 2) of complexes and consistency in the high stability of cis σ-complex intermediates are useful to unravel the deep mechanism of non-alternating copolymerization [72,73].Cis/trans isomerization is the connecting bridge of ethylene coordination and ethylene insertion.The cis σ-complex and trans π-complex are under equilibrium, and isomerization takes place readily in almost all cases.[72,73] Equilibrium with a high kinetic constant cannot directly determine the kinetically favorable step, because CO/ethylene non-alternating copolymerization is a result of kinetic regulation.However, the resulting concentration of the trans π-complex influences the kinetic trend of the monomer insertion to some extent [73].In the case of CO/ethylene non-alternating copolymerization, sequential ethylene insertion must occur in the trans π-complex, and the concentration of the trans π-complex depends on the cis/trans equilibrium constant due to the stability of the cis σ-complex and trans π-complex and the structure of catalysts.More importantly, cis/trans isomerization is also assumed in recent novel examples of CO/ethylene non-alternating copolymerization [63,64], which implies that it might be a concordant insight into the non-alternating pathway.
Charge effects and orbital interactions were also proposed to explain the particularity of phosphine sulfonate ligands, and complexes with neutral charge and atoms with lone pairs covalent bonding Pd promote the multiple insertions of ethylene [2,73,74].Orbital interactions specifically refer to an appropriate stereoelectronic effect of ligands and metal centers.The interactions involving lone pairs in p orbital on the ligated oxygen and dπ Although the destabilization of Pd-acyl β-chelates and decarbonylation could partly explain why non-alternating copolymerization occurs, most mechanisms cannot escape the scope of phenomenological theory.In fact, it is extremely difficult to find a direct connection between the ability of non-alternating copolymerization and the structure of ligands or catalysts.Therefore, there is still no perfect theory to predict new catalyst systems that can achieve non-alternating copolymerization of CO and ethylene.
However, some researchers have made outstanding contributions to exploring the nature of the origin of non-alternating copolymerization [72][73][74][75][76].In different unique polymerizations realized by phosphine sulfonate palladium catalysts, similar cis/trans isomerization (Scheme 2) of complexes and consistency in the high stability of cis σ-complex intermediates are useful to unravel the deep mechanism of non-alternating copolymerization [72,73].Although the destabilization of Pd-acyl -chelates and decarbonylation could partly explain why non-alternating copolymerization occurs, most mechanisms cannot escape the scope of phenomenological theory.In fact, it is extremely difficult to find a direct connection between the ability of non-alternating copolymerization and the structure of ligands or catalysts.Therefore, there is still no perfect theory to predict new catalyst systems that can achieve non-alternating copolymerization of CO and ethylene.
However, some researchers have made outstanding contributions to exploring the nature of the origin of non-alternating copolymerization [72][73][74][75][76].In different unique polymerizations realized by phosphine sulfonate palladium catalysts, similar cis/trans isomerization (Scheme 2) of complexes and consistency in the high stability of cis σ-complex intermediates are useful to unravel the deep mechanism of non-alternating copolymerization [72,73].Cis/trans isomerization is the connecting bridge of ethylene coordination and ethylene insertion.The cis σ-complex and trans π-complex are under equilibrium, and isomerization takes place readily in almost all cases.[72,73] Equilibrium with a high kinetic constant cannot directly determine the kinetically favorable step, because CO/ethylene non-alternating copolymerization is a result of kinetic regulation.However, the resulting concentration of the trans π-complex influences the kinetic trend of the monomer insertion to some extent [73].In the case of CO/ethylene non-alternating copolymerization, sequential ethylene insertion must occur in the trans π-complex, and the concentration of the trans π-complex depends on the cis/trans equilibrium constant due to the stability of the cis σ-complex and trans π-complex and the structure of catalysts.More importantly, cis/trans isomerization is also assumed in recent novel examples of CO/ethylene non-alternating copolymerization [63,64], which implies that it might be a concordant insight into the non-alternating pathway.
Charge effects and orbital interactions were also proposed to explain the particularity of phosphine sulfonate ligands, and complexes with neutral charge and atoms with lone pairs covalent bonding Pd promote the multiple insertions of ethylene [2,73,74].Orbital interactions specifically refer to an appropriate stereoelectronic effect of ligands and metal centers.The interactions involving lone pairs in p orbital on the ligated oxygen and dπ Scheme 2. Non-alternating pathway in CO/ethylene non-alternating copolymerization.
Cis/trans isomerization is the connecting bridge of ethylene coordination and ethylene insertion.The cis σ-complex and trans π-complex are under equilibrium, and isomerization takes place readily in almost all cases.[72,73] Equilibrium with a high kinetic constant cannot directly determine the kinetically favorable step, because CO/ethylene non-alternating copolymerization is a result of kinetic regulation.However, the resulting concentration of the trans π-complex influences the kinetic trend of the monomer insertion to some extent [73].In the case of CO/ethylene non-alternating copolymerization, sequential ethylene insertion must occur in the trans π-complex, and the concentration of the trans π-complex depends on the cis/trans equilibrium constant due to the stability of the cis σ-complex and trans π-complex and the structure of catalysts.More importantly, cis/trans isomerization is also assumed in recent novel examples of CO/ethylene non-alternating copolymerization [63,64], which implies that it might be a concordant insight into the non-alternating pathway.
Charge effects and orbital interactions were also proposed to explain the particularity of phosphine sulfonate ligands, and complexes with neutral charge and atoms with lone pairs covalent bonding Pd promote the multiple insertions of ethylene [2,73,74].Orbital interactions specifically refer to an appropriate stereoelectronic effect of ligands and metal centers.The interactions involving lone pairs in p orbital on the ligated oxygen and d π orbital on palladium atom in the case of phosphine sulfonate ligands palladium catalyst systems (Figure 2).Generally, the SO 3 group withdraws the π-electrons of the adjacent group.When an adjacent group connects directly with an oxygen atom, repulsion between one pair on the oxygen atom and π-electrons on Pd possibly causes an increase in the electron density of palladium.Resultantly, the back-donation from palladium to the antibonding orbital of ethylene is enhanced and the binding affinity of ethylene and metal may be strengthened, thereby enhancing the stabilization of the corresponding trans πcomplex [53,74].orbital on palladium atom in the case of phosphine sulfonate ligands palladium catalyst systems (Figure 2).Generally, the SO3 group withdraws the π-electrons of the adjacent group.When an adjacent group connects directly with an oxygen atom, repulsion between one pair on the oxygen atom and π-electrons on Pd possibly causes an increase in the electron density of palladium.Resultantly, the back-donation from palladium to the antibonding orbital of ethylene is enhanced and the binding affinity of ethylene and metal may be strengthened, thereby enhancing the stabilization of the corresponding trans πcomplex [53,74].Notably, similar stereoelectronic structures exist in both diphosphazane monoxide and phosphinophenolate systems (Figure 3), which are two important catalysts for CO/ethylene non-alternating copolymerization (see Section 4).The striking similarity in stereoelectronic structure is the most critical factor in CO/ethylene non-alternating copolymerization.Orbital interactions provide a new approach to catalyst design and are helpful in developing new CO/ethylene non-alternating copolymerization catalysts.

Non-Alternating Copolymerization Catalysts
Due to the unfavorable kinetics of ethylene sequential insertion, designing catalysts for the synthesis of PKs without a perfect alternating structure is extremely difficult.Until recently, few examples of catalysts achieved ethylene sequential insertion.Phosphinesulfonate Pd catalyst systems, diphosphazane monoxide (PNPO) Pd/Ni catalysts, and phosphinophenolate Ni catalysts represent the three main catalyst systems for CO/ethylene non-alternating copolymerization [50,51,58].In addition, phosphanylferrocene-carboxylate ligand Pd catalysts [77] and zwitterionic Ni catalysts [78] were also reported to synthesize non-alternating PKs with low activity (<15 g PK•mmol −1 •h −1 ).Notably, similar stereoelectronic structures exist in both diphosphazane monoxide and phosphinophenolate systems (Figure 3), which are two important catalysts for CO/ethylene non-alternating copolymerization (see Section 4).The striking similarity in stereoelectronic structure is the most critical factor in CO/ethylene non-alternating copolymerization.Orbital interactions provide a new approach to catalyst design and are helpful in developing new CO/ethylene non-alternating copolymerization catalysts.orbital on palladium atom in the case of phosphine sulfonate ligands palladium catalyst systems (Figure 2).Generally, the SO3 group withdraws the π-electrons of the adjacent group.When an adjacent group connects directly with an oxygen atom, repulsion between one pair on the oxygen atom and π-electrons on Pd possibly causes an increase in the electron density of palladium.Resultantly, the back-donation from palladium to the antibonding orbital of ethylene is enhanced and the binding affinity of ethylene and metal may be strengthened, thereby enhancing the stabilization of the corresponding trans πcomplex [53,74].Notably, similar stereoelectronic structures exist in both diphosphazane monoxide and phosphinophenolate systems (Figure 3), which are two important catalysts for CO/ethylene non-alternating copolymerization (see Section 4).The striking similarity in stereoelectronic structure is the most critical factor in CO/ethylene non-alternating copolymerization.Orbital interactions provide a new approach to catalyst design and are helpful in developing new CO/ethylene non-alternating copolymerization catalysts.

Non-Alternating Copolymerization Catalysts
Due to the unfavorable kinetics of ethylene sequential insertion, designing catalysts for the synthesis of PKs without a perfect alternating structure is extremely difficult.Until recently, few examples of catalysts achieved ethylene sequential insertion.Phosphinesulfonate Pd catalyst systems, diphosphazane monoxide (PNPO) Pd/Ni catalysts, and phosphinophenolate Ni catalysts represent the three main catalyst systems for CO/ethylene non-alternating copolymerization [50,51,58].In addition, phosphanylferrocene-carboxylate ligand Pd catalysts [77] and zwitterionic Ni catalysts [78] were also reported to synthesize non-alternating PKs with low activity (<15 g PK•mmol −1 •h −1 ).

Non-Alternating Copolymerization Catalysts
Due to the unfavorable kinetics of ethylene sequential insertion, designing catalysts for the synthesis of PKs without a perfect alternating structure is extremely difficult.Until recently, few examples of catalysts achieved ethylene sequential insertion.Phosphinesulfonate Pd catalyst systems, diphosphazane monoxide (PNPO) Pd/Ni catalysts, and phosphinophenolate Ni catalysts represent the three main catalyst systems for CO/ethylene non-alternating copolymerization [50,51,58].In addition, phosphanylferrocene-carboxylate ligand Pd catalysts [77] and zwitterionic Ni catalysts [78] were also reported to synthesize non-alternating PKs with low activity (<15 g PK•mmol −1 •h −1 ).

Phosphine-Sulfonate Pd Catalysts
In 2002, Drent first reported the neutral palladium catalysts generated in situ from phosphine-sulfonate ligands [79].The first example of a non-alternating linear CO/ethylene copolymer with successive ethylene incorporation was also reported by Drent by using a phosphine-sulfonate palladium catalyst system [50].
A new series of [P,O] palladium catalysts Pd1~Pd3 (Figure 4) with ortho-alkoxy substituents generated in situ from Pd(OAc) 2 and phosphine-sulfonate ligands were employed for CO/ethylene copolymerization.Despite the activities of copolymerization with these neutral catalysts (49~190 g PK•mmol•Pd −1 •h −1 ) being low compared to classical 1,3-bis(diphenylphosphino)propane (dppp)-based palladium systems, these neutral catalysts produced non-alternating copolymers with 2.4~18.3%non-alt insertions (extra C2 insertion) [50].The non-alternating insertions increase with the steric hindrance of the ortho-alkoxy substituents in the palladium catalytic system (O i Pr > OEt > OMe).Furthermore, the melting points of non-alternating copolymers made by catalysts from Pd1 (234 • C), Pd2 (231 • C) and Pd3 (229 • C) reduce, reflecting the impact of steric hindrance in the palladium catalytic system on the microstructure of the resulting PKs.In 2002, Drent first reported the neutral palladium catalysts generated in situ from phosphine-sulfonate ligands [79].The first example of a non-alternating linear CO/ethylene copolymer with successive ethylene incorporation was also reported by Drent by using a phosphine-sulfonate palladium catalyst system [50].
A new series of [P,O] palladium catalysts Pd1~Pd3 (Figure 4) with ortho-alkoxy substituents generated in situ from Pd(OAc)2 and phosphine-sulfonate ligands were employed for CO/ethylene copolymerization.Despite the activities of copolymerization with these neutral catalysts (49~190 g PK•mmol•Pd −1 •h −1 ) being low compared to classical 1,3bis(diphenylphosphino)propane (dppp)-based palladium systems, these neutral catalysts produced non-alternating copolymers with 2.4~18.3%non-alt insertions (extra C2 insertion) [50].The non-alternating insertions increase with the steric hindrance of the orthoalkoxy substituents in the palladium catalytic system (O i Pr > OEt > OMe).Furthermore, the melting points of non-alternating copolymers made by catalysts from Pd1 (234 °C), Pd2 (231 °C) and Pd3 (229 °C) reduce, reflecting the impact of steric hindrance in the palladium catalytic system on the microstructure of the resulting PKs.The non-alternating CO/ethylene copolymerization using phosphine-sulfonate palladium systems is attributed to the fact that ethylene insertion can take place from the most stable chelate complex "cis σ-complex" via the intermediate "trans π-complex" (see the "Catalytic copolymerization mechanism" section) [73].By examining the kinetic and thermodynamic parameters, Sen discovered that the catalyst exhibits a remarkably minor disparity in its binding affinities for ethylene and carbon monoxide [59].However, the difference in monomer binding affinity alone is not sufficient to explain the degree of nonalternation actually observed in this system.Thus, decarbonylation plays a significant role in the non-alternation.It has been observed that the steric bulk prevents the formation of chelate bonds between the carbonyl oxygens of the PKs chain and the metal center, which facilitates the decarbonylation of an acyl group.This process leads to successive ethylene incorporation and ultimately results in the formation of non-alternating units [59,70,71].
Although successive CO insertions are thermodynamically impossible, CO exhibits a stronger binding affinity to the active palladium species and tends to insert more readily into the Pd-alkyl bond than ethylene.Consequently, obtaining PKs with low CO content is greatly challenging.Sen and coworkers successfully achieved the formation of non-perfect alternating PKs with as low as 10 mol% CO in the Pd1 (Figure 4) catalytic system, although the yields were relatively low [69].Sen and coworkers systematically controlled the monomer feed ratio and reaction temperature, and non-perfect alternating PKs with CO incorporation ranging from 0 to 50 mol% were produced [59].
Muller successfully prepared low-molecular-weight non-alternating PKs (<6 kg•mol −1 ) with varying CO contents (0~50 mol%) in the Pd1 (Figure 4) [65].Segments with high CO density result in domains with strong intermolecular dipole-dipole interactions, which play a dominant role in the phase change behavior of PKs.Additionally, the melt viscosity decreases rapidly with decreasing molecular weight of PKs.The crystallinity of the non-perfect alternating PKs is directly related to the -(C2H4)nsegment length.Additionally, the presence of methyl branches along the chain significantly affects the material The non-alternating CO/ethylene copolymerization using phosphine-sulfonate palladium systems is attributed to the fact that ethylene insertion can take place from the most stable chelate complex "cis σ-complex" via the intermediate "trans π-complex" (see the "Catalytic copolymerization mechanism" section) [73].By examining the kinetic and thermodynamic parameters, Sen discovered that the catalyst exhibits a remarkably minor disparity in its binding affinities for ethylene and carbon monoxide [59].However, the difference in monomer binding affinity alone is not sufficient to explain the degree of non-alternation actually observed in this system.Thus, decarbonylation plays a significant role in the non-alternation.It has been observed that the steric bulk prevents the formation of chelate bonds between the carbonyl oxygens of the PKs chain and the metal center, which facilitates the decarbonylation of an acyl group.This process leads to successive ethylene incorporation and ultimately results in the formation of non-alternating units [59,70,71].
Although successive CO insertions are thermodynamically impossible, CO exhibits a stronger binding affinity to the active palladium species and tends to insert more readily into the Pd-alkyl bond than ethylene.Consequently, obtaining PKs with low CO content is greatly challenging.Sen and coworkers successfully achieved the formation of nonperfect alternating PKs with as low as 10 mol% CO in the Pd1 (Figure 4) catalytic system, although the yields were relatively low [69].Sen and coworkers systematically controlled the monomer feed ratio and reaction temperature, and non-perfect alternating PKs with CO incorporation ranging from 0 to 50 mol% were produced [59].
Muller successfully prepared low-molecular-weight non-alternating PKs (<6 kg•mol −1 ) with varying CO contents (0~50 mol%) in the Pd1 (Figure 4) [65].Segments with high CO density result in domains with strong intermolecular dipole-dipole interactions, which play a dominant role in the phase change behavior of PKs.Additionally, the melt viscosity decreases rapidly with decreasing molecular weight of PKs.The crystallinity of the nonperfect alternating PKs is directly related to the -(C 2 H 4 ) n -segment length.Additionally, the presence of methyl branches along the chain significantly affects the material properties in the solid state, resulting in reduced crystallinity and lower enthalpy of melting.
The unique properties of phosphine-sulfonate palladium catalysts have sparked widespread research interest in the synthesis of non-alternating PKs.Rieger and coworkers reported the palladium catalysts Pd4~Pd6 (Figure 4) with modification of both the benzene ring and phosphine moieties for non-alternating CO/ethylene copolymerizations [67].Pd4 does not produce any significant amounts of polymer under the conditions used, and Pd5 and Pd6 can yield high molecular weight PKs (M w up to 370 kg•mol −1 ) with 2.4~18.3%extra C2 insertions and a melting temperature of 220~230 • C.
The unique properties of phosphine-sulfonate palladium catalysts have sparked widespread research interest in the synthesis of non-alternating PKs.Rieger and coworkers reported the palladium catalysts Pd4~Pd6 (Figure 4) with modification of both the benzene ring and phosphine moieties for non-alternating CO/ethylene copolymerizations [67].Pd4 does not produce any significant amounts of polymer under the conditions used, and Pd5 and Pd6 can yield high molecular weight PKs (Mw up to 370 kg•mol −1 ) with 2.4~18.3%extra C2 insertions and a melting temperature of 220~230 °C.
Rieger further reported the palladium catalysts Pd7~Pd9 (Figure 5) and two monosubstituted palladium catalysts, Pd10 and Pd11 (Figure 5), for CO/ethylene copolymerizations [67].Additionally, Pd7 does not produce PK, but Pd8 and Pd9 exhibit high polymerization activities (2.5~106 g PK•mmol•Pd −1 •h −1 ) and thermal stability compared to the corresponding in situ generated palladium catalysts.Pd9 also exhibits substantial copolymerization activity of 75 g PK•mmol•Pd −1 •h −1 at 200 °C.However, the obtained PK has lower extra C2 insertion (<4.9 mol%) [67].When 2 wt% B(C6F5)3 was used as an activator, the monosubstituted palladium Pd10 and Pd11 (Figure 5) showed increased copolymerization activities (up to 292 g PK•mmol•Pd −1 •h −1 ) to produce PKs with remarkably high extra ethylene insertions (up to 26.4%) [67].In addition to modifying the phosphine moiety, Bianchini and Oberhauser conducted a comparative study on the impact of the backbones of phosphine-sulfonate ligands on the performance of palladium catalysts [68].They investigated the non-alternating CO/ethylene copolymerization catalyzed by palladium catalysts Pd12~Pd15 (Figure 6) with modified phosphine-sulfonate ligands.Pd12 and Pd14 with rigid phenyl backbones exhibited much higher activity (41~607 g PK•mmol•Pd −1 •h −1 ) than Pd13 and Pd15 (0.4~5.4 g PK•mmol•Pd −1 •h −1 ) with the more flexible ligands.The presence of benzoquinone (BQ) oxidant has no appreciable influence on extra C2 insertion while increasing productivity in copolymerization catalyzed by Pd12.Additionally, the former produces copolymers with a significantly higher molecular weight (Mw > 30 kg•mol −1 ).The authors think that the decreased copolymerization activities observed in Pd13 and Pd15 with flexible ligands could be mainly attributed to the faster degradation of catalytically active species.Furthermore, palladium catalysts Pd12 and Pd14 with a rigid backbone produced PKs with higher extra-ethylene insertions (up to 27.8 mol%) compared to Pd13 and Pd15 (0.2~23.2 mol%).In addition to modifying the phosphine moiety, Bianchini and Oberhauser conducted a comparative study on the impact of the backbones of phosphine-sulfonate ligands on the performance of palladium catalysts [68].They investigated the non-alternating CO/ethylene copolymerization catalyzed by palladium catalysts Pd12~Pd15 (Figure 6) with modified phosphine-sulfonate ligands.Pd12 and Pd14 with rigid phenyl backbones exhibited much higher activity (41~607 g PK•mmol•Pd −1 •h −1 ) than Pd13 and Pd15 (0.4~5.4 g PK•mmol•Pd −1 •h −1 ) with the more flexible ligands.The presence of benzoquinone (BQ) oxidant has no appreciable influence on extra C2 insertion while increasing productivity in copolymerization catalyzed by Pd12.Additionally, the former produces copolymers with a significantly higher molecular weight (M w > 30 kg•mol −1 ).The authors think that the decreased copolymerization activities observed in Pd13 and Pd15 with flexible ligands could be mainly attributed to the faster degradation of catalytically active species.Furthermore, palladium catalysts Pd12 and Pd14 with a rigid backbone produced PKs with higher extra-ethylene insertions (up to 27.8 mol%) compared to Pd13 and Pd15 (0.2~23.2 mol%).properties in the solid state, resulting in reduced crystallinity and lower enthalpy of melting.
The unique properties of phosphine-sulfonate palladium catalysts have sparked widespread research interest in the synthesis of non-alternating PKs.Rieger and coworkers reported the palladium catalysts Pd4~Pd6 (Figure 4) with modification of both the benzene ring and phosphine moieties for non-alternating CO/ethylene copolymerizations [67].Pd4 does not produce any significant amounts of polymer under the conditions used, and Pd5 and Pd6 can yield high molecular weight PKs (Mw up to 370 kg•mol −1 ) with 2.4~18.3%extra C2 insertions and a melting temperature of 220~230 °C.
Rieger further reported the palladium catalysts Pd7~Pd9 (Figure 5) and two monosubstituted palladium catalysts, Pd10 and Pd11 (Figure 5), for CO/ethylene copolymerizations [67].Additionally, Pd7 does not produce PK, but Pd8 and Pd9 exhibit high polymerization activities (2.5~106 g PK•mmol•Pd −1 •h −1 ) and thermal stability compared to the corresponding in situ generated palladium catalysts.Pd9 also exhibits substantial copolymerization activity of 75 g PK•mmol•Pd −1 •h −1 at 200 °C.However, the obtained PK has lower extra C2 insertion (<4.9 mol%) [67].When 2 wt% B(C6F5)3 was used as an activator, the monosubstituted palladium Pd10 and Pd11 (Figure 5) showed increased copolymerization activities (up to 292 g PK•mmol•Pd −1 •h −1 ) to produce PKs with remarkably high extra ethylene insertions (up to 26.4%) [67].In addition to modifying the phosphine moiety, Bianchini and Oberhauser conducted a comparative study on the impact of the backbones of phosphine-sulfonate ligands on the performance of palladium catalysts [68].They investigated the non-alternating CO/ethylene copolymerization catalyzed by palladium catalysts Pd12~Pd15 (Figure 6) with modified phosphine-sulfonate ligands.Pd12 and Pd14 with rigid phenyl backbones exhibited much higher activity (41~607 g PK•mmol•Pd −1 •h −1 ) than Pd13 and Pd15 (0.4~5.4 g PK•mmol•Pd −1 •h −1 ) with the more flexible ligands.The presence of benzoquinone (BQ) oxidant has no appreciable influence on extra C2 insertion while increasing productivity in copolymerization catalyzed by Pd12.Additionally, the former produces copolymers with a significantly higher molecular weight (Mw > 30 kg•mol −1 ).The authors think that the decreased copolymerization activities observed in Pd13 and Pd15 with flexible ligands could be mainly attributed to the faster degradation of catalytically active species.Furthermore, palladium catalysts Pd12 and Pd14 with a rigid backbone produced PKs with higher extra-ethylene insertions (up to 27.8 mol%) compared to Pd13 and Pd15 (0.2~23.2 mol%).The ferrocene moiety provides quite a variety of possibilities for electronically modifying catalyst systems derived from chelate ligands.Erker and coworkers reported two in situ phosphine-sulfonate palladium catalysts, Pd16 and Pd17 (Figure 7), and Pd18 complexes with a ferrocene-derived ligand for CO/ethylene copolymerization [80].At a relatively low CO/ethylene feed, these catalysts produced nearly alternating PKs.When the CO/ethylene partial pressure ratio is approximately 1:10, substantially non-alternating PKs were obtained.The overall catalyst activities decreased as the CO partial pressure decreased, but the activities were still quite remarkable (18~159 g PK•mmol•Pd −1 •h −1 ).Pd17 exhibited higher copolymerization activity than Pd16 in spite of a lower percentage of extra ethylene insertions (<1 mol%).The addition of B(C 6 F 5 ) 3 as a Lewis acid activator increased the activity of Pd18 while decreased extra C2 insertion.By precisely controlling the conditions, it is possible to prepare PKs with different amounts of extra ethylene (1~27 mol%) and varying polymer melting temperatures (167~242 The ferrocene moiety provides quite a variety of possibilities for electronically modifying catalyst systems derived from chelate ligands.Erker and coworkers reported two in situ phosphine-sulfonate palladium catalysts, Pd16 and Pd17 (Figure 7), and Pd18 complexes with a ferrocene-derived ligand for CO/ethylene copolymerization [80].At a relatively low CO/ethylene feed, these catalysts produced nearly alternating PKs.When the CO/ethylene partial pressure ratio is approximately 1:10, substantially non-alternating PKs were obtained.The overall catalyst activities decreased as the CO partial pressure decreased, but the activities were still quite remarkable (18~159 g PK•mmol•Pd −1 •h −1 ).Pd17 exhibited higher copolymerization activity than Pd16 in spite of a lower percentage of extra ethylene insertions (<1 mol%).The addition of B(C6F5)3 as a Lewis acid activator increased the activity of Pd18 while decreased extra C2 insertion.By precisely controlling the conditions, it is possible to prepare PKs with different amounts of extra ethylene (1~27 mol%) and varying polymer melting temperatures (167~242 °C).Nozaki also reported phosphine-sulfonate palladium catalysts Pd19~Pd22 (Figure 8) for the copolymerization of ethylene with metal carbonyls as the CO source [60].In contrast to conventional CO/ethylene copolymerization reactions, excellent non-alternating selectivity has been achieved with moderate activity (1.2~54 g PK•mmol•Pd −1 •h −1 ).Linear high molecular weight (44 kg•mol −1 ) polyethylene bearing low content isolated in-chain carbonyls (<4%) was obtained.Although the copolymer retained the properties of polyethylene, it exhibited faster degradation under UV light irradiation compared to pure PE.Jian reported a non-alternating (>99%) terpolymerization of CO with ethylene and fundamental polar monomers using palladium catalysts Pd23~Pd26 (Figure 8) [81].This Nozaki also reported phosphine-sulfonate palladium catalysts Pd19~Pd22 (Figure 8) for the copolymerization of ethylene with metal carbonyls as the CO source [60].In contrast to conventional CO/ethylene copolymerization reactions, excellent non-alternating selectivity has been achieved with moderate activity (1.2~54 g PK•mmol•Pd −1 •h −1 ).Linear high molecular weight (44 kg•mol −1 ) polyethylene bearing low content isolated in-chain carbonyls (<4%) was obtained.Although the copolymer retained the properties of polyethylene, it exhibited faster degradation under UV light irradiation compared to pure PE.The ferrocene moiety provides quite a variety of possibilities for electronically modifying catalyst systems derived from chelate ligands.Erker and coworkers reported two in situ phosphine-sulfonate palladium catalysts, Pd16 and Pd17 (Figure 7), and Pd18 complexes with a ferrocene-derived ligand for CO/ethylene copolymerization [80].At a relatively low CO/ethylene feed, these catalysts produced nearly alternating PKs.When the CO/ethylene partial pressure ratio is approximately 1:10, substantially non-alternating PKs were obtained.The overall catalyst activities decreased as the CO partial pressure decreased, but the activities were still quite remarkable (18~159 g PK•mmol•Pd −1 •h −1 ).Pd17 exhibited higher copolymerization activity than Pd16 in spite of a lower percentage of extra ethylene insertions (<1 mol%).The addition of B(C6F5)3 as a Lewis acid activator increased the activity of Pd18 while decreased extra C2 insertion.By precisely controlling the conditions, it is possible to prepare PKs with different amounts of extra ethylene (1~27 mol%) and varying polymer melting temperatures (167~242 °C).Nozaki also reported phosphine-sulfonate palladium catalysts Pd19~Pd22 (Figure 8) for the copolymerization of ethylene with metal carbonyls as the CO source [60].In contrast to conventional CO/ethylene copolymerization reactions, excellent non-alternating selectivity has been achieved with moderate activity (1.2~54 g PK•mmol•Pd −1 •h −1 ).Linear high molecular weight (44 kg•mol −1 ) polyethylene bearing low content isolated in-chain carbonyls (<4%) was obtained.Although the copolymer retained the properties of polyethylene, it exhibited faster degradation under UV light irradiation compared to pure PE.Jian reported a non-alternating (>99%) terpolymerization of CO with ethylene and fundamental polar monomers using palladium catalysts Pd23~Pd26 (Figure 8) [81].This Jian reported a non-alternating (>99%) terpolymerization of CO with ethylene and fundamental polar monomers using palladium catalysts Pd23~Pd26 (Figure 8) [81].This palladium system effectively prevented the formation of undesired polar monomer chelates such as acrylate (MA, BA), acrylic acid (AA), vinyl ether (VE), and acrylonitrile (AN).High molecular weight linear PE was synthesized with both in-chain isolated carbonyl (>99%) and main-chain functional groups (0.18~2.38 mol%).The incorporation of these low-content isolated carbonyls allows for the photodegradation of the PE.Additionally, the introduction of polar functional groups significantly enhances their surface properties.
Table 3 lists a summary of representative results for non-alternating copolymerization activity, extra C2 insertion, and melting temperature in the phosphine-sulfonate palladium catalyst systems.

Diphosphazane Monoxide Pd/Ni Catalysts
In 2018, Chen discovered a new type of electronic asymmetric diphosphazane monoxide (PNPO) ligand (Figure 5) with multiple modifiable moieties for copolymerization of ethylene with polar monomers [82][83][84].The short-bite ligand platform increases ligand rigidity, and unique electronic asymmetry achieved by a strongly σ-donating phosphine moiety and a weakly σ-donating phosphine oxide moiety is believed to be responsible for its unexpectedly excellent catalytic property.PNPO Ni/Pd catalysts for CO/ethylene nonalternating copolymerization are shown in Figure 9, and the corresponding non-alternating copolymerization results are summarized in Table 4.
moiety are inactive, while Ni6 and Ni7 afforded a copolymer with the highest activity (301 g PK•mmol•Ni −1 •h −1 ).Palladium-based catalysts Pd29~Pd32 and Pd38 were also used to prepare PE with in-chain ketones.The electron-donating substituent on arylamine moieties (Pd29~Pd32) increased both activity and Mn [58,61].Pd38 bearing a strong electrondonating phosphine moiety is the most efficient and afforded copolymers with the highest Mn (93.3 kg•mol −1 ) in 0.1% CO/ethylene feed.

Phosphinophenolate Ni Catalysts
Copolymerization of CO and ethylene catalyzed by Ni complexes is extremely challenging owing to the strong electrophilic nature of Ni.Most Ni catalysts only produced alternating PKs [85][86][87][88][89]. Phosphinophenolate nickel catalysts were first developed for the copolymerization of ethylene and acrylates [90,91].In 2021, Mecking reported CO/ethylene non-alternating copolymerization using phosphinophenolate Ni complexes (Ni9~Ni14) to yield in-chain ketone PE materials.In 0.2 mol % CO feed, PE with in-chain ketones was obtained with a Tm low of 134 °C [51].This material maintains the excellent mechanical and processing properties of traditional PE and also possesses the degradability of PKs [51].Phosphinophenolate Ni catalysts for CO/ethylene non-alternating copolymerization are summarized in Figure 11, and the corresponding non-alternating copolymerization results are summarized in Table 5. Liu has reported Pd41~Pd50 for non-alternating copolymerization of CO and ethylene [63].Compared with Pd32, Pd41~Pd43 bearing an aliphatic substituent on the amine moiety showed non-alternating copolymerization with almost two times higher activity and higher carbonyl content.Pd44 bearing benzylamine and Ar 3 (2,6-OMeC 6 H 3 ) (Figure 10) is highly efficient (activity up to 124.1 g PK•mmol•Pd −1 •h −1 ) for CO/ethylene non-alternating copolymerization.Liu also found that steric hindrance and electron-donating ability of the substituent on phosphine oxide moiety are beneficial to extra ethylene insertion, thus Pd45~Pd49 afforded PKs with relatively high extra ethylene insertion (12.2%) [63].In addition, Pd50 bearing -NMe 2 on the phosphine oxide moiety has a different complexation mode, and it afforded PKs with low activity and carbonyl content.
Liu also developed a series of PNPO nickel/palladium catalysts, and PE with inchain ketones was synthesized by Ni1~Ni8, Pd29~Pd32, and Pd38 [61].In a very low CO/ethylene feed of 0.2%, copolymers were produced in low carbonyl content and low T m (<140 • C).Both steric hindrance and the electronic nature of ligands have significant impacts on activity, M n , and carbonyl content.With increasing electron-donating ability of the substituents at the N-aryl moiety from Ni1 to Ni4, the resultant copolymers' M n decreases, but their carbonyl content and activity exhibited uncertain regularity.Ni5 and Ni8 bearing the strongest electron-donating and electron-withdrawing substituents on phosphine moiety are inactive, while Ni6 and Ni7 afforded a copolymer with the highest activity (301 g PK•mmol•Ni −1 •h −1 ).Palladium-based catalysts Pd29~Pd32 and Pd38 were also used to prepare PE with in-chain ketones.The electron-donating substituent on arylamine moieties (Pd29~Pd32) increased both activity and M n [58,61].Pd38 bearing a strong electron-donating phosphine moiety is the most efficient and afforded copolymers with the highest M n (93.3 kg•mol −1 ) in 0.1% CO/ethylene feed.

Phosphinophenolate Ni Catalysts
Copolymerization of CO and ethylene catalyzed by Ni complexes is extremely challenging owing to the strong electrophilic nature of Ni.Most Ni catalysts only produced alternating PKs [85][86][87][88][89]. Phosphinophenolate nickel catalysts were first developed for the copolymerization of ethylene and acrylates [90,91].In 2021, Mecking reported CO/ethylene non-alternating copolymerization using phosphinophenolate Ni complexes (Ni9~Ni14) to yield in-chain ketone PE materials.In 0.2 mol % CO feed, PE with in-chain ketones was obtained with a T m low of 134 • C [51].This material maintains the excellent mechanical and processing properties of traditional PE and also possesses the degradability of PKs [51].Phosphinophenolate Ni catalysts for CO/ethylene non-alternating copolymerization are summarized in Figure 11, and the corresponding non-alternating copolymerization results are summarized in Table 5.Generally, phosphinophenolate Ni complexes have a relatively complex structure and multiple modification modes [51,64].Unlike phosphine sulfonate Pd catalysts, the rate-determining step of alternating and non-alternating steps in phosphinophenolate Nicatalyzed CO/ethylene copolymerization were identified as the opening of the six-membered C,O-chelate by ethylene coordination and cis/trans isomerization of an alkyl-olefin intermediate, respectively (Figure 12) [64].Short duration copolymerization experiments and theoretical studies were systematically studied, and the details of the connection between the catalyst structure and rate-determining step were unraveled.The steric effect at the aromatic rings on the phosphine moiety apically coordinated to the metal center significantly impacts the free energy barrier of cis/trans isomerization and the free energy barrier of the ethylene coordination step (Figure 12) [64].Simultaneously, an η 2 -coordination of a P-bound aromatic moiety axially oriented to the metal center, which is considered as a crucial feature of catalysts, modulates the competition between alternating and nonalternating pathways.Generally, phosphinophenolate Ni complexes have a relatively complex structure and multiple modification modes [51,64].Unlike phosphine sulfonate Pd catalysts, the rate-determining step of alternating and non-alternating steps in phosphinophenolate Ni-catalyzed CO/ethylene copolymerization were identified as the opening of the sixmembered C,O-chelate by ethylene coordination and cis/trans isomerization of an alkylolefin intermediate, respectively (Figure 12) [64].Short duration copolymerization experiments and theoretical studies were systematically studied, and the details of the connection between the catalyst structure and rate-determining step were unraveled.The steric effect at the aromatic rings on the phosphine moiety apically coordinated to the metal center significantly impacts the free energy barrier of cis/trans isomerization and the free energy barrier of the ethylene coordination step (Figure 12) [64].Simultaneously, an η 2 -coordination of a P-bound aromatic moiety axially oriented to the metal center, which is considered as a crucial feature of catalysts, modulates the competition between alternating and non-alternating pathways.
In general, the influence of catalyst structure on competition can be summarized as follows.(1) Bulkier steric hindrance, enhanced by the η 2 -coordination mentioned above, impedes the inversion of the intermediate conformation during copolymerization, thereby increasing the energy barrier of cis/trans isomerization and finally weakening the tendency for non-alternating polymerization.(2) The electronic effect of ligands directly determines the electron density at the Ni center.The strong electrophilicity of Ni easily causes a very stable resting state, which prohibits both alternating and non-alternating pathways.In contrast, strong electron-donating groups lead to low electrophilicity Ni, which is favorable for alternating polymerization because of the easy opening of the six-membered In general, the influence of catalyst structure on competition can be summarized as follows.(1) Bulkier steric hindrance, enhanced by the η 2 -coordination mentioned above, impedes the inversion of the intermediate conformation during copolymerization, thereby increasing the energy barrier of cis/trans isomerization and finally weakening the tendency for non-alternating polymerization.(2) The electronic effect of ligands directly determines the electron density at the Ni center.The strong electrophilicity of Ni easily causes a very stable resting state, which prohibits both alternating and non-alternating pathways.In contrast, strong electron-donating groups lead to low electrophilicity Ni, which is favorable for alternating polymerization because of the easy opening of the sixmembered C,O-chelate [51,64].Interestingly, phenolate substitution has few effects on the microstructure of copolymers compared with phosphine substituents [64].
In addition, Nozaki also reported phosphinophenolate Ni catalysts for the synthesis of PE with in-chain ketones using metal carbonyls as a carbonyl source [62].High selectivity to isolated carbonyl and higher activity were realized compared to the Pd catalysts reported by them.

Conclusions and Outlook
Aliphatic PKs generated from the copolymerization of CO and ethylene have attracted considerable attention over the last decades due to their unique properties and environmental friendliness.Alternating PKs have a high Tm and insolubility, while PKs without a perfect alternating structure have better processability.However, the synthesis of PKs without a perfect alternating structure is extremely difficult because of the unfavorable kinetics of ethylene sequential insertion.Phosphine-sulfonate Pd catalyst systems, PNPO Pd/Ni catalysts, and phosphinophenolate Ni catalysts represent the three main catalysts for CO/ethylene non-alternating copolymerization.Catalytic activity and the carbonyl content of PKs are two important parameters to evaluate catalysts.Interestingly, stereoelectronic structure and the orbital interactions involving lone pairs in the p orbital on the oxygen donor and dπ orbital on the metal atom are observed in three kinds of catalysts, which open a window for the design of non-alternating ethylene/CO copolymerization catalysts.
Despite significant breakthroughs in non-alternating copolymerization of CO in recent years, there are still several challenges for future development in this field: (1) modulating the carbonyl content of PKs by CO/ethylene feed in copolymerization often causes In addition, Nozaki also reported phosphinophenolate Ni catalysts for the synthesis of PE with in-chain ketones using metal carbonyls as a carbonyl source [62].High selectivity to isolated carbonyl and higher activity were realized compared to the Pd catalysts reported by them.

Conclusions and Outlook
Aliphatic PKs generated from the copolymerization of CO and ethylene have attracted considerable attention over the last decades due to their unique properties and environmental friendliness.Alternating PKs have a high T m and insolubility, while PKs without a perfect alternating structure have better processability.However, the synthesis of PKs without a perfect alternating structure is extremely difficult because of the unfavorable kinetics of ethylene sequential insertion.Phosphine-sulfonate Pd catalyst systems, PNPO Pd/Ni catalysts, and phosphinophenolate Ni catalysts represent the three main catalysts for CO/ethylene non-alternating copolymerization.Catalytic activity and the carbonyl content of PKs are two important parameters to evaluate catalysts.Interestingly, stereoelectronic structure and the orbital interactions involving lone pairs in the p orbital on the oxygen donor and d π orbital on the metal atom are observed in three kinds of catalysts, which open a window for the design of non-alternating ethylene/CO copolymerization catalysts.
Despite significant breakthroughs in non-alternating copolymerization of CO in recent years, there are still several challenges for future development in this field: (1) modulating the carbonyl content of PKs by CO/ethylene feed in copolymerization often causes a rapid decrease in activity.(2) There is no widely acceptable theory to explain the relationship between the structure of catalysts and non-alternating copolymerization, therefore designing new catalysts seems to only depend on a large number of experiments.(3) Noble palladium catalyst represents the most successful catalytic system, while the replacement of palladium by nickel or other non-noble transition metals poses significant challenges.

Table 1 .
Microstructure and Tm of three kinds of PKs.

Scheme 1 .
Scheme 1. Presented mechanisms in the formation of alternating PKs and PKs without a perfect alternating structure catalyzed by Pd complexes.

Scheme 1 .
Scheme 1. Presented mechanisms in the formation of alternating PKs and PKs without a perfect alternating structure catalyzed by Pd complexes.

Scheme 1 .
Scheme 1. Presented mechanisms in the formation of alternating PKs and PKs without a perfect alternating structure catalyzed by Pd complexes.

Figure 12 .
Figure 12.Competition and rate-determining step in Ni catalyzed synthesis of PE with in-chain ketones.

Figure 12 .
Figure 12.Competition and rate-determining step in Ni catalyzed synthesis of PE with in-chain ketones.

Table 2 .
Structural fragments and NMR shifts of PKs without a perfect alternating structure.
a /207.0 b

Table 2 .
Structural fragments and NMR shifts of PKs without a perfect alternating structure.
Int. J.Mol.Sci.2024, 25, x FOR PEER REVIEW 3 of 19 including non-perfect alternating PKs and PE with in-chain ketones.The chain structure of PKs without a perfect alternating structure, catalytic copolymerization mechanism, and Ni/Pd catalysts are summarized.

Table 1 .
Microstructure and Tm of three kinds of PKs.

Table 2 .
Structural fragments and NMR shifts of PKs without a perfect alternating structure.
a /207.0 b

Table 1 .
Microstructure and Tm of three kinds of PKs.

Table 2 .
Structural fragments and NMR shifts of PKs without a perfect alternating structure.
a /207.0 b

Table 1 .
Microstructure and Tm of three kinds of PKs.

Table 2 .
Structural fragments and NMR shifts of PKs without a perfect alternating structure.

Table 1 .
Microstructure and Tm of three kinds of PKs.

Table 2 .
Structural fragments and NMR shifts of PKs without a perfect alternating structure.

Table 1 .
Microstructure and Tm of three kinds of PKs.

Table 2 .
Structural fragments and NMR shifts of PKs without a perfect alternating structure.

Table 3 .
CO/ethylene non-alternating copolymerization results using phosphine-sulfonate palladium catalysts.Activity: in units of g PK mmol•Pd −1 •h −1 .bTotalmol % ethylene of copolymer involved in non-alternation, calculated from13C NMR spectra.c Determined by DSC.d Not determined.e B(C 6 F 5 ) 3 is used as the activator, BQ: benzoquinone as the oxidant. a

AC d Mn e PDI e Tm f Ref
13CO was used to enhance sensitivity.bActivity: in units of g PK•(mmol•Ni) −1 •h −1 .cCarbonylcontentdeterminedbyIRspectroscopy; in brackets: carbonyl content calculated from13C NMR spectroscopy by integration of the13C labeled C=O signals.dIC:isolated carbonyl; NA: non-alternating carbonyl; AC: alternating carbonyl; see Table2for specification.e Mn in units of kg•mol −1 , determined by GPC in 1,2-dichlorobenzene at 160 °C.
a f Determined by DSC.g Not determined.
a 13 CO was used to enhance sensitivity.bActivity: in units of g PK•(mmol•Ni) −1 •h −1 .cCarbonylcontentdeter-mined by IR spectroscopy; in brackets: carbonyl content calculated from13C NMR spectroscopy by integration of the13C labeled C=O signals.d IC: isolated carbonyl; NA: non-alternating carbonyl; AC: alternating carbonyl; see Table 2 for specification.e M n in units of kg•mol −1 , determined by GPC in 1,2-dichlorobenzene at 160 • C. f Determined by DSC.g Not determined.