Next Article in Journal
A Study on Aqueous Dispersing of Carbon Black Nanoparticles Surface-Coated with Styrene Maleic Acid (SMA) Copolymer
Previous Article in Journal
Selective Solvolysis of Bio-Based PU-Coated Fabric
 
 
Search for Articles:
Title / Keyword
Author / Affiliation / Email
Journal
Article Type
 
 
Advanced Search
 
Section
Special Issue
Volume
Issue
Number
Page
 
Journals
Polymers
Volume 14
Issue 24
10.3390/polym14245453
polymers-logo
Submit to this Journal Review for this Journal Propose a Special Issue
► Article Menu

Article Menu

share Share announcement Help format_quote Cite question_answer Discuss in SciProfiles thumb_up
...
Endorse textsms
...
Comment
first_page
settings
Order Article Reprints
Font Type:
Arial Georgia Verdana
Font Size:
Aa Aa Aa
Line Spacing:
Column Width:
Background:
Article

Chiral Polymers from Norbornenes Based on Renewable Chemical Feedstocks

by
Ivan V. Nazarov
1,
Danil P. Zarezin
1,
Ivan A. Solomatov
1,
Anastasya A. Danshina
2,3,
Yulia V. Nelyubina
2,
Igor R. Ilyasov
4 and
Maxim V. Bermeshev
1,*
1
A.V. Topchiev Institute of Petrochemical Synthesis, RAS, 29 Leninskiy Pr., 119991 Moscow, Russia
2
A.N. Nesmeyanov Institute of Organoelement Compounds, Russian Academy of Sciences, Vavilov Street 28, 119991 Moscow, Russia
3
Moscow Institute of Physics and Technology, National Research University, Institutskiy Per., 9, 141700 Dolgoprudny, Russia
4
Nelubin Institute of Pharmacy, Sechenov First Moscow State Medical University, Trubetskaya Str. 8/2, 119991 Moscow, Russia
*
Author to whom correspondence should be addressed.
Polymers 2022, 14(24), 5453; https://doi.org/10.3390/polym14245453
Submission received: 5 November 2022 / Revised: 28 November 2022 / Accepted: 7 December 2022 / Published: 13 December 2022
(This article belongs to the Topic Polymers from Renewable Resources)
Browse Figures
Versions Notes

Abstract

:
Optically active polymers are of great interest as materials for dense enantioselective membranes, as well as chiral stationary phases for gas and liquid chromatography. Combining the versatility of norbornene chemistry and the advantages of chiral natural terpenes in one molecule will open up a facile route toward the synthesis of diverse optically active polymers. Herein, we prepared a set of new chiral monomers from cis-5-norbornene-2,3-dicarboxylic anhydride and chiral alcohols of various natures. Alcohols based on cyclic terpenes ((-)-menthol, (-)-borneol and pinanol), as well as commercially available alcohols (S-(-)-2-methylbutanol-1, S-(+)-3-octanol), were used. All the synthesized monomers were successfully involved in ring-opening metathesis polymerization, affording polymers in high yields (up to 96%) and with molecular weights in the range of 1.9 × 105–5.8 × 105 (Mw). The properties of the metathesis polymers obtained were studied by TGA and DSC analysis, WAXD, and circular dichroism spectroscopy. The polymers exhibited high thermal stability and good film-forming properties. Glass transition temperatures for the prepared polymers varied from −30 °C to +139 °C and, therefore, the state of the polymers changed from rubbery to glassy. The prepared polymers represent a new attractive platform of chiral polymeric materials for enantioselective membrane separation and chiral stationary phases for chromatography.

1. Introduction

Synthetic optically active polymers are of great interest both in academic and industrial fields. On the one hand, such polymers are widely studied and used in asymmetric catalysis [1,2,3] and as materials for dense enantioselective membranes [4,5,6], chiral stationary phases for gas and liquid chromatography [7,8,9], and also for mimicking biological properties [10,11,12]. On the other hand, these polymers are suitable objects for systematic structure–property study. There are three main approaches to achieving the optical activity of polymers. The first way is the formation of chiral centers in main chains [13,14]. The second one is the introduction of chiral moieties in side chains of polymers [15,16] and in the case of the third way, optical activity appears due to a supramolecular structure [17,18].
Metathesis polymerization of various monomers is a powerful tool for obtaining all three types of polymers. At the same time, ring-opening metathesis polymerization (ROMP) of functionalized norbornenes is the most versatile methodology in the design and preparation of various polymers with the required architecture [19,20,21]. There are several significant benefits of this tool. Norbornene-type monomers can be readily prepared by using well-known cycloaddition (e.g., the Diels–Alder and [2 + 2 + 2]-cycloaddition reactions) and other reactions [22,23,24,25], and these monomers show high reactivity in ROMP polymerization. Moreover, such monomers can be polymerized according to three different mechanisms, affording polymers with different structures of main chains (Figure 1) [19,26,27,28,29]. In turn, well-defined Grubbs catalysts exhibit good tolerance towards various functional groups and allow the control of tacticity, configuration of backbones, the composition of copolymers, molecular weights, and molecular weight distributions.
Some chiral polymers from optically pure isomers of norbornene derivatives were earlier described. The most investigated among these monomers are N-substituted norbornene-2,3-dicarboximides with a chiral group at nitrogen atom [15,30] and norbornenes bearing ester [31,32,33] or ether [34,35] moiety between norbornene skeleton and a chiral fragment. At the same time, monoterpenes, such as α- and β-pinenes, borneol, and menthol are attractive synthetic building blocks and the source of available chiral moieties that are obtained from renewable feedstock. They are widely represented in nature. Therefore, it seems an attractive strategy to combine a norbornene moiety as a polymerizable part with a fragment of a terpene as the source of chirality in the same molecule to develop new optically active polymers for the structure–property study.
Here we report the preparation and ROMP polymerization of a new set of norbornene-type monomers based on alcohols from cyclic terpenes ((-)-menthol, (-)-borneol, and pinanol) as well as commercially available alcohols (S-(-)-2-methylbutanol-1, S-(+)-3-octanol). As a result, a series of high-molecular-weight polymers with good film-forming properties was successfully obtained. The prepared polymers represent a new attractive platform of chiral polymeric materials for enantioselective membrane separation and chiral stationary phases for chromatography. The properties of the metathesis polymers obtained were studied by TGA and DSC analysis, WAXD, and circular dichroism spectroscopy.

2. Materials and Methods

2.1. Materials

(-)-Menthol, (-)-borneol, S-(+)-3-octanol, S-(-)-2-methylbutanol-1, the 2nd generation Grubbs catalysts, dicyclopentadiene, 1,2,4-trichlorbenzene, maleic anhydride, Et3N, SOCl2, and cis-5-norbornene-endo-2,3-dicarboxylic anhydride (endo-NDA) were purchased from commercial suppliers (Sigma-Aldrich, ABCR GmbH, and TCI) and used as received unless otherwise noted. Methylene chloride and 1,2-dichloroethane were distilled over CaH2 under argon atmosphere and stored over molecular sieves (4 Å). Toluene was distilled in argon atmosphere and stored over molecular sieves (4 Å). ((1R,2S,5R)-6,6-Dimethylbicyclo[3.1.1]heptan-2-yl)methanol (pinanol) was prepared according to the procedure described earlier [36].

2.2. Physico-Chemical Characterization

NMR spectra were recorded on a Bruker Ascend 400 spectrometer at 400.1 MHz (1H), 100.6 MHz (13C) and on a Bruker MSL-300 spectrometer at 300 MHz (1H). Chemical shifts (δ) are reported in parts per million (ppm) relative to the reference (residual CHCl3 signal) for 1H and 13C NMR spectra. Each sample of a polymer for NMR analysis was dissolved in CDCl3 up to a concentration of 10%.
Gel-permeation chromatography (GPC) analysis of the polymers was performed on Agilent 1280 Infinity II system with a differential refractometer (THF as the eluent, flow rate 0.3 mL/min). Molecular mass and polydispersity were calculated by standard procedure relative to monodispersed polystyrene standards.
Calorimetric measurements were conducted using a “Mettler” TA-4000 differential scanning calorimeter (Mettler Toledo, Giesen, Germany) at a heating rate of 20 °C/min under argon. TGA measurements were carried out on “TGA/DSC 1” (Mettler Toledo, Polaris Parkway, OH, USA) in argon and in air at the heating rate of 10 °C/min from 30 to 1000 °C.
Wide-angle X-ray diffraction (WAXD) data were obtained using a two-coordinate AXS detector (Bruker, Bremen, Germany) and Cu Kα emission (wavelength of 0.154 nm).
Specific rotation was measured using KRÜSS P3000 polarimeter in CHCl3 or THF (HPLC grade). Circular dichroism (CD) spectra of the monomers and polymers were measured in chloroform or THF at the concentration of 1 mg/mL. Spectra were recorded with spectropolarimeter J810 (Jasco, Hachioji city, Tokio, Japan) in the 220–450 nm range (50 nm/min, 1 nm slit width) in 0.1 cm path-length quartz cells with a detachable window (Hellma, Jena, Germany). The baseline spectrum was recorded from pure chloroform or THF.
The density of polymer films was calculated by the hydrostatic weighing method according to the following procedure. A sample of the film was weighed on analytical balance (mdry). Thin copper wire was hung on a beam over the balance. The sample was fixed on the lower end of the wire, immersed in the beaker with methanol placed on the balance, and weighed (m1). Then, the sample was withdrawn and the free wire end immersed in methanol was weighed (m2). The density of the film sample was calculated by the formula: d = dS mdry/(mdry – (m1 – m2)), where dS = 0.791 g/mL is the density of methanol.
X-ray diffraction data for M2 were collected at 120 K with a Bruker APEXII DUO CCD diffractometer, using graphite monochromated Cu-Kα radiation (λ = 1.54178 Å, ω-scans), while those for M1, at 100 K with a Bruker Quest D8 CMOS diffractometer, using graphite monochromated Mo-Kα radiation (λ = 0.71073 Å, ω-scans). Structures were solved using Intrinsic Phasing with the ShelXT [37] structure solution program in Olex2 [38] and then refined with the XL [39] refinement package using Least-Squares minimization against F2 in the anisotropic approximation for non-hydrogen atoms. Positions of hydrogen atoms were calculated, and they were refined in the isotropic approximation within the riding model. Crystal data and structure refinement parameters are given in Table S1. CCDC 2213611 (M2) and 2213612 (M1) contain supplementary crystallographic information for this paper.
High-resolution mass spectra were recorded on Bruker maXis QTOF (tandem quarrupole/time-of-flight mass analyzer) mass spectrometers equipped with an ESI source. The m/z scanning range was 50–1600. External calibration of the mass scale was carried out using a low-concentration calibration solution “Tuning mix” (Agilent Technologies, Santa Clara, California, USA). Samples were injected using a 500 μL Hamilton RN 1750 syringe (Hamilton, Biel, Switzerland). The measurements were carried out in the positive ion mode (+) (grounded spray needle, −4500 V high-voltage capillary; HV End Plate Offset: −500 V). Nitrogen was used as a nebulizer gas (1.0 bar) and dry gas (4.0 L/min, 200 °C). The data were processed using the Bruker Data Analysis 4.0 software.

2.3. Film Preparation

The polymer films were prepared by casting from 5 wt.% chloroform solution of a polymer. The solution was poured into a steel cylinder with a diameter of 7 cm and a stretched cellophane bottom. The solvent was allowed to evaporate slowly at room temperature to yield the desired polymer film. After the formation of the films, the cellophane was detached, and the films were dried under vacuum at room temperature to a constant weight. A thermal treatment was not applied. The thickness of the films formed was in the range of 40–60 µm.

2.4. Synthetic Part

Cis-5-norbornene-exo-2,3-dicarboxylic anhydride (exo-NDA). In a 1000 mL two-necked round bottom flask fitted with reflux, dropping funnel with dicyclopentadiene (DCPD, 122.4 mL, 0.909 mol) and a magnetic stirring bar, was placed 300 mL of 1,2,4-trichlorbenzene and 178 g of maleic anhydride (1.818 mol). The solution was heated to 200 °C and DCPD added dropwise over 20 min. The solution acquired a yellow color, which changed to dark brown upon further heating. The resulting solution was stirred for 4 h at 200 °C. After that, it was cooled down and left overnight after the addition of n-hexane. The next day, the crystal precipitate was formed in the flask. The precipitate was separated and recrystallized 4 times from the minimum amount of benzene. The white crystalline substance was obtained (54.6 g, yield 18%). M.p.—145–149 °C
  • 1H NMR (300 MHz, CDCl3, δ, ppm): 1.50 (dd, 2H, RCH2, J = 10.20); 2.97 (s, 2H); 3.42 (s, 2H); 6.30 (s, 2H, R-CH=CH-R).
  • 13C NMR (100 MHz, CDCl3, δ, ppm): 44.07; 46.82; 48.71; 137.91; 171.59.

2.5. General Procedure for the Synthesis of Monomers M1–M3

The synthesis of M1. The first step was performed similarly to the previously described procedure with minor differences [40]. A 250 mL round-bottom flask was equipped with a magnetic stirring bar, and then was filled with 13.4 g (82 mmol) of exo-NDA, 200 mL of dry toluene, 29.5 mL of triethylamine (210 mmol) and 57.56 g (370 mmol) of (-)-menthol. The mixture was stirred for 96 h (24 for borneol ester) at 55 °C with the conversion control by 1H NMR spectroscopy. The remaining solvent and triethylamine were evaporated at a rotary evaporator. The resulting residue was redissolved in 125 mL of diethyl ether. The solution was washed with 10% hydrochloric acid (3 × 120 mL). The aqueous layer was extracted with diethyl ether (5 × 200 mL). The organic layers were combined and extracted with saturated K2CO3 solution (4 × 250 mL). The resulting aqueous phase was washed once with diethyl ether (150 mL). Then, the aqueous phase was acidified with hydrochloric acid and extracted with methylene chloride (5 × 200 mL). The combined organic layers were dried with anhydrous magnesium sulfate filtered and the remaining solvents were evaporated on a rotary evaporator. As a result, 26.24 g (96% yield) of crude (-)-menthyl ester of exo-norbornene dicarboxylic acid was obtained.
The second and third steps. In a 100 mL round-bottom flask equipped with a magnetic stirring bar, 11.34 g (35 mmol) of (-)-menthyl exo-norbornene dicarboxylic acid monoester, 25.5 mL (351 mmol) of thionyl chloride, and 80 mL of absolute toluene were placed with a couple of drops of DMF. The mixture was stirred for 4 h at 90 °C. The remaining excess of thionyl chloride was removed under vacuum, and the resulting product was dissolved in 150 mL of dry toluene and 3.66 mL of pyridine (1.3 eq.). (-)-Menthol (4.66 g, 30 mmol) was added to the prepared solution. The resulting mixture was heated to 90 °C and stirred for two hours. Then, toluene was evaporated on a rotary evaporator. The resulting product was recrystallized from ethanol. The yield of M1 was 13.82 g (86% at this stage). The crystals of M1 suitable for X-ray analysis were prepared by the slow evaporation of methanol solution of M1. [α]D25 = −75 deg·mL·g−1·dm−1 in CHCl3 (C = 1). ESI-(+)HRMS, m/z: 459.3472, calcd for C29H47O4: 459.3469 [M + H]+.
  • 1H NMR (400 MHz, CDCl3, δ, ppm): 6.26–6.24 (m, 2H, R-HC=CH-R), 4.61–4.76 (m, 2H), 3.15–3.14 (m, 1H), 3.05–3.04 (m, 1H), 2.63–2.62 (m, 1H), 2.55–2.54 (m, 1H), 2.13–2.04 (m, 3H), 2.03–1.86 (m, 2H), 1.76–1.60 (m, 4H), 1.56–1.30 (m, 5H), 1.62–0.76 (m, 24H).
  • 13C NMR (100 MHz, CDCl3, δ, ppm): 172.93–172.78, 138.15–137.77, 74.52–74.24, 47.53, 47.34, 46.95, 46.88, 46.78, 45.68, 45.19, 40.68, 40.23, 34.33, 31.49–31.35, 26.19, 25.96, 23.42, 23.35, 22.07, 20.95, 16.57, 16.25.
  • Monomer M2
Endo-NDA was used instead of exo-NDA for M2 synthesis. The yield of M2 was 76%. The crystals of M2 suitable for X-ray analysis were prepared by the slow evaporation of the methanol solution of M2. [α]D20 = −125 deg·mL·g−1·dm−1 in CHCl3 (C = 1). ESI-(+)HRMS, m/z: 459.3461, calcd for C29H47O4: 459.3469 [M + H]+.
  • 1H NMR (400 MHz, CDCl3, δ, ppm): 6.28 (br. S., 1H), 6.20 (br.s., 1H), 4.68–4.53 (m, 2H), 3.25–3.15 (m, 4H), 2.05–1.96 (m, 2H), 1.95–1.82 (m, 2H), 1.68–1.62 (m, 4H), 1.47–1.23 (m, 7H), 1.10–0.96 (m, 2H), 0.94–0.79 (m, 17H), 0.78–0.70 (m, 6H).
  • 13C NMR (100 MHz, CDCl3, δ, ppm): 171.98, 171.79, 135.32, 134.52, 74.36, 74.00, 48.62, 48.18, 48.14, 47.48, 47.04, 46.78, 40.95, 40.84, 34.50, 34.45, 31.59, 31.45, 26.25, 25.96, 23.42, 23.37, 22.19, 21.09, 21.06, 16.46, 16.36.
  • Monomer M3
The yield of M3 was 72%. [α]D20 = −42 deg·mL·g−1·dm−1 in CHCl3 (C = 1). ESI-(+)HRMS, m/z: 455.3156, calcd for C29H43O4: 455.3156 [M + H]+.
  • 1H NMR (400 MHz, CDCl3, δ, ppm): 6.24 (br. S., 2H), 3.11–3.07 (m, 2H), 2.68–2.63 (m, 2H), 2.43–2.24 (m, 2H), 2.21–2.14 (m, 1H), 2.00–1.85 (m, 2H), 1.81–1.63 (m, 4H), 1.55–1.46 (m, 1H), 1.36–1.12 (m, 5H), 1.12–0.96 (m, 2H), 0.92–0.82 (m, 20H).
  • 13C NMR (100 MHz, CDCl3, δ, ppm): 173.62, 173.61, 137.99, 137.94, 80.40, 80.15, 48.96, 48.58, 47.82, 47.70, 47.38, 45.91, 45.35, 44.86, 44.84, 36.87, 36.14, 28.03, 27.24, 27.22, 19.71, 18.85, 13.65, 13.51.

2.6. General Procedure for the Synthesis of Monomers M4–M6

Synthesis of M5. A 50 mL one-neck flask was equipped with a reflux condenser, 0.93 g (0.57 mmol) exo-NDA, (S)-(-)-2-methylbutanol 1.1 g (1.25 mmol), 0.06 g (0.61 mmol) para-toluenesulfonic acid, and 30 mL toluene(abs) as a solvent. Molecular sieves (4 Å) were used as a drying agent. The reaction mixture was refluxed for 14 h and the conversion was monitored by 1H NMR spectroscopy. The mixture was cooled and washed with saturated solution of K2CO3 (2 × 15 mL). After that, the organic layer was washed with water (15 mL), brine (15 mL) and dried over MgSO4. Then, it was filtered and the toluene was evaporated on a rotary evaporator. The product was purified by silica gel column chromatography using hexanes/ethyl acetate (40/1) as an eluent. The product was obtained as a colorless viscous oil (1.3 g, 71% yield). [α]D20 = +7 deg·mL·g−1·dm−1 in THF (C = 1). ESI-(+)HRMS, m/z: 321.2038, calcd for C29H29O4: 321.2060 [M + H]+.
  • 1H NMR (300 MHz, CDCl3, δ, ppm): 6.15 (br. s, 2H, R-CH=CH-R), 3.96–3.67 (M, 4H), 3.02 (s, 2H), 2.57 (s, 2H), 2.07 (m, 2H), 1.67–1.55 (m, 2H), 1.45–1.29 (m, 3H), 1.23–1.03 (m, 2H), 0.92–0.77 (m, 12H).
  • 13C NMR (100 MHz, CDCl3, δ, ppm): 172.99, 137.36, 68.82, 46.77, 45.13, 44.80, 33.50, 33.46, 25.48, 15.87, 15.83, 10.66, 10.61.
  • Monomer M4
The monomer yield was 68%. [α]D20 = −11 deg·mL·g−1·dm−1 in CHCl3 (C = 1). ESI-(+)HRMS, m/z: 455.3153, calcd for C29H43O4: 455.3156 [M + H]+.
  • 1H NMR (400 MHz, CDCl3, δ, ppm): 6.20 (s, 2H, R-CH=CH-R), 4.08–4.02 (m, 2H), 3.94–3.89 (m, 2H), 3.08–3.05 (m, 2H), 2.60–2.57 (m, 2H), 2.38–2.30 (m, 4H), 2.13–2.08 (m, 1H), 1.95–1.84 (m, 10H), 1.52–1.41 (m, 3H), 1.19–1.17 (m, 6H), 1.00–0.96 (m, 6H), 0.94–0.90 (m, 2H).
  • 13C NMR (100 MHz, CDCl3, δ, ppm): 173.72, 173.67, 138.09, 138.07, 65.51, 69.30, 47.49, 47.47, 45.90, 45.82, 45.73, 45.54, 46.40, 43.18, 41.39, 41.37, 40.41, 40.30, 38.64, 33.12, 33.07, 27.99, 27.97, 25.98, 23.39, 23.34, 18.94, 18.81.
  • Monomer M6
The monomer yield was 54%. [α]D20 = +4 deg·mL·g−1·dm−1 in CHCl3 (C = 1). ESI-(+)HRMS, m/z: 407.3155, calcd for C25H43O4: 407.3156 [M + H]+.
  • 1H NMR (400 MHz, CDCl3, δ, ppm): 6.17 (s, 2H, R-CH=CH-R), 4.74–4.71 (m, 2H), 3.03–3.02 (m, 2H), 2.54–2.53 (m, 2H), 2.11–2.09 (m, 1H), 1.52–1.42 (m, 9H), 1.37–1.17 (m, 12H), 0.87–0.83 (m, 12H).
  • 13C NMR (100 MHz, CDCl3, δ, ppm): 173.15, 138.03, 137.99, 75.84, 75.79, 47.45, 47.37, 46.19, 46.08, 45.33, 33.21, 33.13, 31.92, 31.82, 26.55, 26.54, 25.05, 24.93, 22.62, 14.09, 14.06, 9.63, 9.50.
  • Epoxide based on M5
  • 1H NMR (400 MHz, CDCl3, δ, ppm): 4.03–3.72 (M, 4H), 3.18 (s, 2H), 2.82 (s, 2H), 2.78 (s, 2H), 1.76–0.84 (m, 20H).
  • 13C NMR (100 MHz, CDCl3, δ, ppm): 172.11, 69.68, 50.68, 47.08, 40.97, 34.02, 33.98, 26.03, 23.27, 16.43, 16.40, 11.23, 11.19.
  • MS (EI, m/z (intensity, %)): 338 (2%, M+), 181 (60%, C9H9O4+).

2.7. General Procedure of ROMP Polymerization (MP1–MP6)

The synthesis of MP5. The monomer M5 (3.12 g, 9.7 mmol) was dissolved in 15.9 mL of absolute 1,2-dichloroethane and the solution of the 2-st generation Grubbs catalyst 3.52 mL (0.0129 mmol, 3.36 × 10−3 M) was added to the monomer solution at stirring. The stirring was continued for 2 h at 45 °C. The polymerization was terminated by the addition of ethyl vinyl ether with following stirring for 10 min. Then, the polymer solution was precipitated by methanol containing the inhibitor (2,2′-methylenebis(6-tert-butyl-4-methylphenol)). The polymer was separated, washed with several portions of methanol, and dried in vacuum. The polymer was twice reprecipitated by methanol from the chloroform solution and dried in vacuum to a constant weight (3.00 g, 96% yield). Mw = 4.57 × 105, Mw/Mn = 2.2. [α]D22 = 9 deg·mL·g−1·dm−1 in THF (C = 1).
  • 1H NMR (400 MHz, CDCl3, δ, ppm): 5.51–5.23 (m, 2H, HRC=CRH), 3.94–0.72 (m, 31H).
  • 13C NMR (100 MHz, CDCl3, δ, ppm): 178.14–178.10 (C=O), 133.37–131.80, 69.74–69.30, 53.91–52.62, 45.71–44.80, 41.25–39.45, 34.27–33.96, 26.31–26.05, 16.72–16.33, 11.41–11.23.
  • Polymer MP1
The polymer yield was 96%. Mw = 4.88 × 105, Mw/Mn = 2.1. [α]D22 = −59 deg·mL·g−1·dm−1 in CHCl3 (C = 1).
  • 1H NMR (400 MHz, CDCl3, δ, ppm): 5.55–4.51 (m, 4H), 3.56–0.56 (m, 42H).
  • 13C NMR (100 MHz, CDCl3, δ, ppm): 172.87–171.44, 134.54–131.65, 74.50–74.00, 54.31–52.07, 47.55–44.51, 41.26–39.18, 34.72–34.13, 31.90–31.32, 26.62–25.70, 23.86–23.18, 22.61–21.82, 24.41–20.85, 16.97–16.10.
  • Polymer MP2
The polymer yield was 74%. Mw = 1.9 × 105, Mw/Mn = 1.6. [α]D22 = −64 deg·mL·g−1·dm−1 in CHCl3 (C = 1).
  • 1H NMR (400 MHz, CDCl3, δ, ppm): 5.74–5.28 (m, 2H), 4.81–4.55 (m, 2H), 3.31–0.45 (m, 42H).
  • 13C NMR (100 MHz, CDCl3, δ, ppm): 171.94–170.91, 132.14–130.53, 75.12–73.81, 52.21–15.62.
  • Polymer MP3
The polymer yield was 94%. Mw = 4.69 × 105, Mw/Mn = 2.1. [α]D22 = −34 deg·mL·g−1·dm−1 in CHCl3 (C = 1).
  • 1H NMR (400 MHz, CDCl3, δ, ppm): 5.66–5.12 (m, 2H), 5.01–4.71 (m, 2H), 3.31–0.45 (m, 38H).
  • 13C NMR (100 MHz, CDCl3, δ, ppm): 173.15–171.92, 133.42–131.48, 80.68–79.12, 53.62–13.52.
  • Polymer MP4
The polymer yield was 95%. Mw = 5.8 × 105, Mw/Mn = 2.9. [α]D22 = −11 deg·mL·g−1·dm−1 in CHCl3 (C = 1).
  • 1H NMR (400 MHz, CDCl3, δ, ppm): 5.50–5.11 (m, 2H, HRC=CRH), 4.12–0.77 (m, 40H).
  • 13C NMR (100 MHz, CDCl3, δ, ppm): 172.94–172.52, 133.20–132.26, 69.29–69.27, 53.58–52.59, 45.25–38.60, 33.20–33.00, 28.12–27.95, 25.98–25.96, 23.42–23.41, 19.05–18.95
  • Polymer MP6
The polymer yield was 92%. Mw = 2.69 × 105, Mw/Mn = 2.2. [α]D22 = +4 deg·mL·g−1·dm−1 in CHCl3 (C = 1).
  • 1H NMR (400 MHz, CDCl3, δ, ppm): 5.54–5.13 (m, 2H), 4.81–4.64 (m, 2H), 3.53–0.76 (m, 38H).
  • 13C NMR (100 MHz, CDCl3, δ, ppm): 172.93–171.85, 134.12–131.61, 76.16–75.43, 54.30–52.16, 46.07–44.27, 41.03–39.23, 33.73–32.86, 32.16–31.58, 27.12–26.25, 25.50–24.51, 22.95–22.43, 14.55–13.79, 9.97–9.39.

2.8. Synthesis of Polymer MP7

The monomer M1 (0.30 g, 0.66 mmol) was dissolved in 0.80 mL of absolute toluene. RuCl3·3H2O (3.5 mg, 0.011 mmol) was dissolved in 1.0 mL of EtOH (abs) and the solution was stirred for 15 min. After that, the solution of M1 in toluene was added to the solution of RuCl3 in ethanol. The resulting mixture was heated for 48 h at 75 °C. Then, the reaction mixture was precipitated by methanol containing the inhibitor (2,2′-methylenebis(6-tert-butyl-4-methylphenol)). The polymer was separated, washed with several portions of methanol, and dried in vacuum. The polymer was twice reprecipitated by methanol from the chloroform solution and dried in vacuum to a constant weight. The polymer yield was 18% (52.5 mg). Mw = 2.9 × 105, Mw/Mn = 2.6. [α]D22 = −46 deg·mL·g−1·dm−1 in CHCl3 (C = 1). Tg = 81 °C.
  • 1H NMR (400 MHz, CDCl3, δ, ppm): 5.54–5.37 (m, 2H), 4.75–458 (m, 2H), 3.10–0.55 (m, 42H).

3. Results and Discussion

3.1. Synthesis of Monomers

Herein we designed and synthesized two sets of new chiral di-substituted norbornene-type monomers (Scheme 1 and Scheme 2). The chiral groups in these monomers are attached to norbornene moiety via ester linkages. As the source of norbornene moiety, cis-5-norbornene-exo-2,3-dicarboxylic anhydride (exo-NDA) was chosen due to its preparative availability and high reactivity. As starting materials for introducing chiral fragments, renewable optically active alcohols ((-)-menthol, (-)-borneol, and pinanol), as well as commercial chiral primary and secondary alcohols, were used.
The required monomers were readily prepared in moderate or good yields according to one- and three-step procedures (Table 1). Primary and less sterically hindered alcohols reacted directly with exo-NDA with the formation of the corresponding diesters (Scheme 2). This scheme was found to be inefficient for the preparation of diesters of cis-5-norbornene-exo-2,3-dicarboxylic acid based on (-)-menthol and (-)-borneol. Therefore, an alternative way for the synthesis of the corresponding diesters from (-)-menthol and (-)-borneol was realized (Scheme 1). By the usage of this scheme, a diester M2, which is an isomer of M1, was also obtained from endo-NDA and (-)-menthol to evaluate the influence of exo-/endo-isomerism on the properties of resulting polymers. It is worth noting that intermediates formed in the first step of the three-step procedure can be isolated as mixtures of the diastereomers (Scheme 1).
All the synthesized monomers were isolated as individual compounds. Their structure and purity were analyzed by 1H, 13C NMR spectroscopy (Figures S1–S11), and HRMS (Figures S13–S18). In the case of solid monomers M1 and M2, X-ray analysis was additionally performed (Figure 2, Table S1), which confirmed the expected structures of the studied monomers. The specific optical rotations for the monomers were nonzero (Table 1). The optical activity of these compounds was also confirmed by circular dichroism (CD) spectroscopy, showing a Cotton effect (Figures S31–S35).
Interestingly, the synthesized diesters showed a tendency to be slowly oxidized with atmospheric oxygen. We found that M5 was oxidized with atmospheric oxygen for several months, affording the corresponding epoxide in the quantitative yield (Scheme 3, Figure 3 and Figure S12). This is different from the related N-substituted imides of cis-5-norbornene-exo-2,3-dicarboxylic acid which are stable in the air [41]. Therefore, it is desirable to store such diesters in an inert atmosphere.

3.2. Ring-Opening Metathesis Polymerization

Ring-opening metathesis polymerization of the synthesized monomers was studied in the presence of the second-generation Grubbs catalyst (Scheme 4). All the monomers exhibited high reactivity. ROMP polymerization of diesters of cis-5-norbornene-exo-2,3-dicarboxylic acid proceeded for a couple of hours at catalyst loadings of 0.1–0.2 mol.% with the formation of soluble high-molecular weight products in good and high yields (Table 2). For the synthesized polymers, relatively narrow values of molecular weight distributions were found.
The reactivity of the endo-isomer was noticeably lower than that of the exo-isomer (M2 vs. M1, Table 2). Nevertheless, we succeeded to obtain ROMP polymer from M2 with high Mw (above 1 × 105) in a good yield. The analysis of the prepared ROMP polymers with NMR-spectroscopy confirmed the expected structure (Figure 4 and Figures S19–S30). The cis-/trans-ratio of double bonds in monomer units of these polymers (Figure 5 and Figure 6) was analyzed with 1H NMR spectroscopy. The signals of protons at cis- and trans-double bonds for these polymers are at around 5.2 ppm and 5.35 ppm, correspondingly. This was confirmed by the synthesis of the isomeric ROMP polymer from M1 (polymer MP7, Figure 6) in the presence of RuCl3·3H2O/ethanol catalytic system, which gives ROMP polymers with predominantly trans-double bonds (>90%). The studied ROMP polymers obtained over the second generation Grubbs catalyst contained a little more cis- than trans-double bonds (53–60%, e.g., the cis-/trans-double bond ratio was 54/46 for MP1).
These ROMP polymers are optically active as it was established by the measurements of the specific optical rotations (Table 2) and by CD spectroscopy (Figures S31–S35). The cis/trans-ratio of double bonds has an effect on optical activity. For instance, MP1 and MP7 are isomeric ROMP polymers differing in the ratio of cis/trans-double bonds (>98% trans-double bonds in MP7 and 46% of trans-double bonds in MP1). The specific optical rotations are −59 deg·mL·g−1·dm−1 and −46 deg·mL·g−1·dm−1 for MP1 and MP7, correspondingly. It should be noted that the cis/trans-ratio of double bonds can affect the secondary structure of the obtained polymers, forming, for example, a helix in the case of polymers containing predominantly one type of double bond. This study is in progress now.
The resulting ROMP polymers showed good solubility in THF and chloroform while swelling in many other common organic solvents (Table 3). The good solubility and high molecular weights allowed preparing free-standing and robust thin films from these polymers (Figure 7).
The density of the obtained polymers exceeded 1.0 g/cm3 (Table 4), which is unusual because, for related halogen-free polymers, the density is typically less than 1 g/cm3. Despite the high density, the fraction free volume (FFV) for these polymers is in the range of 16–17%, which is higher than the values typical for polymers with low free volume [42]. It is possible that the obtained FFV values can be explained by the presence of bulky and rigid side-substituents in such polymers, which create free-volume elements near them.
The synthesized polymers showed glass transition temperatures (Tg) in the range of −30 to +139 °C (Table 2), depending on the substituents’ nature. At the same time, there were no melting peaks in the DSC curves (Figure S36), which indicates the amorphous nature of the prepared polymers. The ROMP polymers with long flexible alkyl groups had the lowest values of Tg, while the highest Tg was observed for the ROMP polymer with bulky and rigid borneol moieties in side chains. Interestingly, isomeric polymers based on exo-NDA and endo-NDA diesters (MP1 vs. MP2) showed very different Tg values, and MP2 derived from endo-NDA had a higher Tg value, evidencing that MP2 possesses more rigid polymeric backbones.
TGA analysis of the synthesized ROMP polymers showed their high thermal stability (Figure 8, Figures S37–S42). The decomposition temperatures (5 wt.% loss) in argon and in air were close and exceeded 300 °C. For some of the resulting polymers, a small weight loss (1–2%) was observed around 180–200 °C, probably due to traces of sorbed water (Figure 8b). Char yields at 1000 °C were close to zero, which indicates the almost complete decomposition of the polymers at high temperatures.
The state of polymers is another important characteristic that determines the performance of a polymer in many applications. According to the WAXD study, all the synthesized polymers are amorphous (Figure 9). WAXD patterns for MP1, MP2, MP5 and MP6 are represented by two broad signals. At the same time, for MP3 and MP4 the second peak was not observed and WAXD patterns are represented by one intensive broad peak at larger 2θ angles. The WAXD patterns of MP1 were the same before and after heating the polymer sample, and the intensity of the peak in WAXD patterns only slightly changed after heating (Figure S43), confirming the amorphous nature of the polymer. It is worth noting that usually there is a single broad peak for conventional amorphous glassy polymers in their WAXD patterns. Two signals in WAXD patterns of MP1, MP2, MP5 and MP6 are not usual for amorphous glassy polymers. It was shown that the signals at higher 2θ angles are related to intrasegmental interactions and the signals at lower 2θ angles to intersegmental interactions [44,45]. Therefore, it seems that both intra- and inter-segmental interactions are significant in the case of MP1, MP2, MP5 and MP6. Within this group of polymers, d1- and d2-distances are practically the same (Table 5). In turn, MP3 and MP4 had d1-distances close to d2-distances for MP1, MP2, MP5 and MP6 polymers. It should be noted, although there is no clear trend between WAXD data and real porosity, the polymers with larger d-spacings often have a more porous structure [46]. Thus, a more porous structure in the case of MP1, MP2, MP5 and MP6 can be expected.
The amorphous nature of the synthesized polymers, good film-forming properties, and high thermal stability, combined with the facile method of the synthesis, make these polymers attractive for the detailed study of their properties in the future as promising materials for dense enantioselective membranes and chiral stationary phases for chromatography.

4. Conclusions

A set of new optically active polymers was developed based on chiral norbornene-type monomers. The desired monomers were readily prepared in good yields by the esterification of cis-5-norbornene-2,3-dicarboxylic anhydride with alcohols from the renewable sources ((-)-menthol, (-)-borneol, and pinanol) and with commercially available alcohols (S-(-)-2-methylbutanol-1, S-(+)-3-octanol). ROMP polymerization of these monomers over the second-generation Grubbs catalyst afforded the metathesis polymers in good yields with high-molecular weights. The synthesized ROMP polymers showed high thermal stability. They had good film-forming properties, giving free-standing thin films from solutions suitable for studying membrane properties. The properties of the polymers strongly depended both on the nature of side groups and the type of their bonding with monomer units (exo-/endo-isomerism). Glass transition temperatures for the prepared polymers can be varied in a wide range (from −30 °C to +139 °C) and, therefore, the state of the polymers can be changed from rubbery to glassy. Thus, it is possible to fine-tune the properties of these polymers to achieve the desired characteristics by changing the nature of the side chains. The prepared polymers represent a new attractive platform of chiral polymeric materials for enantioselective membrane separation and chiral stationary phases for chromatography.

Supplementary Materials

The following supporting information can be downloaded at: https://www.mdpi.com/article/10.3390/polym14245453/s1, Figures S1–S12: NMR spectra of monomers; Figures S13–S18: HRMS spectra of monomers; Figures S19–S30: NMR spectra of polymers; Figures S31–S35: CD spectra of monomers and polymers; Figures S36–S42: DSC and TGA curves for polymers; Figure S43: WAXD patterns of MP1; Table S1: Crystal data and structure refinement details for M1 and M2.

Author Contributions

Visualization, formal analysis, investigation, I.V.N.; investigation, D.P.Z.; investigation, I.A.S.; investigation, A.A.D.; investigation, Y.V.N.; investigation, I.R.I.; conceptualization, validation, methodology, and writing, M.V.B. All authors have read and agreed to the published version of the manuscript.

Funding

The design and synthesis of ROMP polymers were supported by the Russian Science Foundation (grant no. 20-13-00428). The preparation of pinanol was carried out within the State Program of TIPS RAS. X-ray diffraction data were collected using the equipment of Center for molecular composition studies of INEOS RAS with financial support from the Ministry of Science and Higher Education of the Russian Federation (Contract/agreement No. 075-00697-22-00).

Institutional Review Board Statement

Not applicable.

Informed Consent Statement

Not applicable.

Data Availability Statement

NMR, CD spectra, and TGA curves of the monomers and the polymers are available free of charge as a file of Supplementary Materials.

Acknowledgments

This work was performed using the equipment of the Shared Research Center «Analytical center of deep oil processing and petrochemistry of TIPS RAS».

Conflicts of Interest

The authors declare no conflict of interest.

References

  1. Bolm, C.; Tanyeli, C.; Grenz, A.; Dinter, C.L. ROMP-Polymers in Asymmetric Catalysis: The Role of the Polymer Backbone. Adv. Synth. Catal. 2002, 344, 649–656. [Google Scholar] [CrossRef]
  2. Abdelkawy, M.A.; Davin, C.; Aly, E.-S.A.; El-Badawi, M.A.; Itsuno, S. Chiral Polyureas Derived Cinchona Alkaloids: Highly Efficient Bifunctional Organocatalysts for the Asymmetric Michael Addition Reaction. ChemistrySelect 2021, 6, 11971–11979. [Google Scholar] [CrossRef]
  3. Wali Ullah, M.; Haraguchi, N. Asymmetric Diels-Alder Reaction Catalyzed by Facile Recoverable Ionically Core-Corona Polymer Microsphere-Immobilized MacMillan Catalyst. ChemistrySelect 2022, 7, e202202568. [Google Scholar] [CrossRef]
  4. Han, H.; Liu, W.; Xiao, Y.; Ma, X.; Wang, Y. Advances of enantioselective solid membranes. New J. Chem. 2021, 45, 6586–6599. [Google Scholar] [CrossRef]
  5. Vedovello, P.; Marcio Paranhos, C.; Fernandes, C.; Elizabeth Tiritan, M. Chiral polymeric membranes: Recent applications and trends. Sep. Purif. Technol. 2022, 280, 119800. [Google Scholar] [CrossRef]
  6. Choi, H.-J.; Ahn, Y.-H.; Koh, D.-Y. Enantioselective Mixed Matrix Membranes for Chiral Resolution. Membranes 2021, 11, 279. [Google Scholar] [CrossRef]
  7. Guntari, S.N.; Nam, E.; Pranata, N.N.; Chia, K.; Wong, E.H.H.; Blencowe, A.; Goh, T.K.; Caruso, F.; Qiao, G.G. Fabrication of Chiral Stationary Phases via Continuous Assembly of Polymers for Resolution of Enantiomers by Liquid Chromatography. Macromol. Mater. Eng. 2014, 299, 1285–1291. [Google Scholar] [CrossRef] [Green Version]
  8. Teixeira, J.; Tiritan, M.E.; Pinto, M.M.M.; Fernandes, C. Chiral Stationary Phases for Liquid Chromatography: Recent Developments. Molecules 2019, 24, 865. [Google Scholar] [CrossRef] [Green Version]
  9. Betzenbichler, G.; Huber, L.; Kräh, S.; Morkos, M.-L.K.; Siegle, A.F.; Trapp, O. Chiral stationary phases and applications in gas chromatography. Chirality 2022, 34, 732–759. [Google Scholar] [CrossRef]
  10. Wang, L.; Lu, N.; Huang, S.; Wang, M.; Chen, X.-M.; Yang, H. Optically Active Nucleobase-Functionalized Polynorbornenes Mimicking Double-Helix DNA. CCS Chem. 2021, 3, 1787–1796. [Google Scholar] [CrossRef]
  11. Dana, D.M.; Yitzhak, M. Biomimetic Polymers for Chiral Resolution and Antifreeze Applications. In On Biomimetics; Lilyana, D.P., Ed.; IntechOpen: Rijeka, Croatia, 2011. [Google Scholar]
  12. Green, J.J.; Elisseeff, J.H. Mimicking biological functionality with polymers for biomedical applications. Nature 2016, 540, 386–394. [Google Scholar] [CrossRef] [PubMed]
  13. De Rosa, C.; Di Girolamo, R.; Talarico, G. Expanding the Origin of Stereocontrol in Propene Polymerization Catalysis. ACS Catal. 2016, 6, 3767–3770. [Google Scholar] [CrossRef]
  14. Emmerich, A.; Daniliuc, C.G.; Studer, A. Synthesis of Polymers Bearing a Chiral Backbone via Stereospecific Ionic Ring-Opening Polymerization of Chiral Donor-Acceptor Cyclopropanes. Macromol. Rapid Commun. 2021, 42, 2100030. [Google Scholar] [CrossRef]
  15. Mizuta, K.; Fukutomi, S.; Yamabuki, K.; Onimura, K.; Oishi, T. Ring-opening metathesis polymerization of N-substituted-5-norbornene-2,3-dicarboximides in the presence of chiral additives. Polym. J. 2010, 42, 534–539. [Google Scholar] [CrossRef] [Green Version]
  16. Zang, Y.; Aoki, T.; Teraguchi, M.; Kaneko, T.; Ma, L.; Jia, H.; Miao, F. Synthesis of Well-Defined Chiral Oligopinanylsiloxane Graft Copoly(phenylacetylene)s Using the Macromonomer Method and Their Enantioselective Permeability. ACS Appl. Polym. Mater. 2020, 2, 853–861. [Google Scholar] [CrossRef]
  17. Zhou, Y.; Zhang, C.; Zhou, Z.; Zhu, R.; Liu, L.; Bai, J.; Dong, H.; Satoh, T.; Okamoto, Y. Influence of different sequences of l-proline dipeptide derivatives in the pendants on the helix of poly(phenylacetylene)s and their enantioseparation properties. Polym. Chem. 2019, 10, 4810–4817. [Google Scholar] [CrossRef]
  18. Daeffler, C.S.; Miyake, G.M.; Li, J.; Grubbs, R.H. Partial Kinetic Resolution of Oxanorbornenes by Ring-Opening Metathesis Polymerization with a Chiral Ruthenium Initiator. ACS Macro Lett. 2014, 3, 102–104. [Google Scholar] [CrossRef] [Green Version]
  19. Ogba, O.M.; Warner, N.C.; O'Leary, D.J.; Grubbs, R.H. Recent advances in ruthenium-based olefin metathesis. Chem. Soc. Rev. 2018, 47, 4510–4544. [Google Scholar] [CrossRef] [Green Version]
  20. Alentiev, D.A.; Bermeshev, M.V. Design and Synthesis of Porous Organic Polymeric Materials from Norbornene Derivatives. Polym. Rev. 2021, 62, 400–437. [Google Scholar] [CrossRef]
  21. Ponkratov, D.O.; Shaplov, A.S.; Vygodskii, Y.S. Metathesis Polymerization in Ionic Media. Polym. Sci. Ser. C 2019, 61, 2–16. [Google Scholar] [CrossRef]
  22. Petrov, V.A.; Vasil'ev, N.V. Synthetic chemistry of quadricyclane. Curr. Org. Synth. 2006, 3, 215–259. [Google Scholar] [CrossRef]
  23. Houk, K.N.; Liu, F.; Yang, Z.; Seeman, J.I. Evolution of the Diels–Alder Reaction Mechanism since the 1930s: Woodward, Houk with Woodward, and the Influence of Computational Chemistry on Understanding Cycloadditions. Angew. Chem. Int. Ed. 2021, 60, 12660–12681. [Google Scholar] [CrossRef] [PubMed]
  24. Guseva, M.A.; Alentiev, D.A.; Bermesheva, E.V.; Zamilatskov, I.A.; Bermeshev, M.V. The selective hydrosilylation of norbornadiene-2,5 by monohydrosiloxanes. RSC Adv. 2019, 9, 33029–33037. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  25. Sundell, B.J.; Lawrence, J.A.; Harrigan, D.J.; Lin, S.; Headrick, T.P.; O’Brien, J.T.; Penniman, W.F.; Sandler, N. Exo-selective, Reductive Heck Derived Polynorbornenes with Enhanced Molecular Weights, Yields, and Hydrocarbon Gas Transport Properties. ACS Macro Lett. 2020, 9, 1363–1368. [Google Scholar] [CrossRef]
  26. Bermeshev, M.V.; Chapala, P.P. Addition polymerization of functionalized norbornenes as a powerful tool for assembling molecular moieties of new polymers with versatile properties. Prog. Polym. Sci. 2018, 84, 1–46. [Google Scholar] [CrossRef]
  27. Bermesheva, E.V.; Wozniak, A.I.; Andreyanov, F.A.; Karpov, G.O.; Nechaev, M.S.; Asachenko, A.F.; Topchiy, M.A.; Melnikova, E.K.; Nelyubina, Y.V.; Gribanov, P.S.; et al. Polymerization of 5-Alkylidene-2-norbornenes with Highly Active Pd–N-Heterocyclic Carbene Complex Catalysts: Catalyst Structure–Activity Relationships. ACS Catal. 2020, 10, 1663–1678. [Google Scholar] [CrossRef]
  28. Bermeshev, M.V.; Bulgakov, B.A.; Genaev, A.M.; Kostina, J.V.; Bondarenko, G.N.; Finkelshtein, E.S. Cationic Polymerization of Norbornene Derivatives in the Presence of Boranes. Macromolecules 2014, 47, 5470–5483. [Google Scholar] [CrossRef]
  29. García-Loma, R.; Albéniz, A.C. Vinylic Addition Polynorbornene in Catalysis. Asian J. Org. Chem. 2019, 8, 304–315. [Google Scholar] [CrossRef]
  30. Coles, M.P.; Gibson, V.C.; Mazzariol, L.; North, M.; Teasdale, W.G.; Williams, C.M.; Zamuner, D. Amino acid derived homochiral polymers via ring-opening metathesis polymerisation. J. Chem. Soc. Chem. Commun. 1994, 21, 2505–2506. [Google Scholar] [CrossRef]
  31. Sutthasupa, S.; Terada, K.; Sanda, F.; Masuda, T. Ring-opening metathesis polymerization of amino acid-functionalized norbornene diester monomers. Polymer 2007, 48, 3026–3032. [Google Scholar] [CrossRef]
  32. Rosebrugh, L.E.; Marx, V.M.; Keitz, B.K.; Grubbs, R.H. Synthesis of Highly Cis, Syndiotactic Polymers via Ring-Opening Metathesis Polymerization Using Ruthenium Metathesis Catalysts. J. Am. Chem. Soc. 2013, 135, 10032–10035. [Google Scholar] [CrossRef] [PubMed] [Green Version]
  33. Choinopoulos, I.; Koinis, S.; Pitsikalis, M. Synthesis and characterization of chiral poly(l-lactide-b-hexyl isocyanate) macromonomers with norbornenyl end groups and their homopolymerization through ring opening metathesis polymerization to afford polymer brushes. J. Polym. Sci. Part A Polym. Chem. 2017, 55, 1102–1112. [Google Scholar] [CrossRef]
  34. Fadlallah, S.; Peru, A.A.M.; Flourat, A.L.; Allais, F. A straightforward access to functionalizable polymers through ring-opening metathesis polymerization of levoglucosenone-derived monomers. Eur. Polym. J. 2020, 138, 109980. [Google Scholar] [CrossRef]
  35. Fadlallah, S.; Peru, A.A.M.; Longé, L.; Allais, F. Chemo-enzymatic synthesis of a levoglucosenone-derived bi-functional monomer and its ring-opening metathesis polymerization in the green solvent Cyrene™. Polym. Chem. 2020, 11, 7471–7475. [Google Scholar] [CrossRef]
  36. Souto, J.A.; Stockman, R.A.; Ley, S.V. Development of a flow method for the hydroboration/oxidation of olefins. Org. Biomol. Chem. 2015, 13, 3871–3877. [Google Scholar] [CrossRef] [Green Version]
  37. Sheldrick, G. Crystal structure refinement with SHELXL. Acta Crystallogr. Sect. C 2015, 71, 3–8. [Google Scholar] [CrossRef] [Green Version]
  38. Dolomanov, O.V.; Bourhis, L.J.; Gildea, R.J.; Howard, J.A.K.; Puschmann, H. OLEX2: A complete structure solution, refinement and analysis program. J. Appl. Crystallogr. 2009, 42, 339–341. [Google Scholar] [CrossRef]
  39. Sheldrick, G. A short history of SHELX. Acta Crystallogr. Sect. A 2008, 64, 112–122. [Google Scholar] [CrossRef] [Green Version]
  40. Bolm, C.; Atodiresei, I.; Schiffers, I. Asymmetric alcoholysis of meso-anhydrides mediated by alkaloids. Org. Synth. 2005, 82, 120–125. [Google Scholar] [CrossRef]
  41. Bermesheva, E.V.; Nazarov, I.V.; Kataranova, K.D.; Khrychikova, A.P.; Zarezin, D.P.; Melnikova, E.K.; Asachenko, A.F.; Topchiy, M.A.; Rzhevskiy, S.A.; Bermeshev, M.V. Cocatalyst versus precatalyst impact on the vinyl-addition polymerization of norbornenes with polar groups: Looking at the other side of the coin. Polym. Chem. 2021, 12, 6355–6362. [Google Scholar] [CrossRef]
  42. Yushkin, A.; Grekhov, A.; Matson, S.; Bermeshev, M.; Khotimsky, V.; Finkelstein, E.; Budd, P.M.; Volkov, V.; Vlugt, T.J.H.; Volkov, A. Study of glassy polymers fractional accessible volume (FAV) by extended method of hydrostatic weighing: Effect of porous structure on liquid transport. React. Funct. Polym. 2015, 86, 269–281. [Google Scholar] [CrossRef]
  43. Askadskii, A.A. Computational Materials Science of Polymers; Cambridge International Science Publishing Ltd.: Cambridge, UK, 2003; p. 16. [Google Scholar]
  44. Wilks, B.R.; Chung, W.J.; Ludovice, P.J.; Rezac, M.R.; Meakin, P.; Hill, A.J. Impact of average free-volume element size on transport in stereoisomers of polynorbornene. I. Properties at 35 °C. J. Polym. Sci. Part B Polym. Phys. 2003, 41, 2185–2199. [Google Scholar] [CrossRef]
  45. Wilks, B.R.; Chung, W.J.; Ludovice, P.J.; Rezac, M.E.; Meakin, P.; Hill, A.J. Structural and free-volume analysis for alkyl-substituted palladium-catalyzed poly(norbornene): A combined experimental and Monte Carlo investigation. J. Polym. Sci. Part B Polym. Phys. 2006, 44, 215–233. [Google Scholar] [CrossRef]
  46. Gringolts, M.; Bermeshev, M.; Yampolskii, Y.; Starannikova, L.; Shantarovich, V.; Finkelshtein, E. New High Permeable Addition Poly(tricyclononenes) with Si(CH3)3 Side Groups. Synthesis, Gas Permeation Parameters, and Free Volume. Macromolecules 2010, 43, 7165–7172. [Google Scholar] [CrossRef]
Polymers 14 05453 g001 550
Figure 1. The ways of norbornene-type monomers polymerization.
Figure 1. The ways of norbornene-type monomers polymerization.
Polymers 14 05453 g001
Polymers 14 05453 sch001 550
Scheme 1. The synthesis of monomers M1–M3 (*M2 is endo-isomer of M1).
Scheme 1. The synthesis of monomers M1–M3 (*M2 is endo-isomer of M1).
Polymers 14 05453 sch001
Polymers 14 05453 sch002 550
Scheme 2. The synthesis of monomers M4–M6.
Scheme 2. The synthesis of monomers M4–M6.
Polymers 14 05453 sch002
Polymers 14 05453 g002 550
Figure 2. The structure of M1 (a) and M2 (b) according to X-ray analysis.
Figure 2. The structure of M1 (a) and M2 (b) according to X-ray analysis.
Polymers 14 05453 g002
Polymers 14 05453 sch003 550
Scheme 3. The oxidation of M5 during storage in air.
Scheme 3. The oxidation of M5 during storage in air.
Polymers 14 05453 sch003
Polymers 14 05453 g003 550
Figure 3. 1H NMR spectrum of the epoxide based on M5 (CDCl3).
Figure 3. 1H NMR spectrum of the epoxide based on M5 (CDCl3).
Polymers 14 05453 g003
Polymers 14 05453 sch004 550
Scheme 4. Ring-opening metathesis polymerization of the prepared monomers (*MP2 was obtained from M2 (endo-isomer of M1)).
Scheme 4. Ring-opening metathesis polymerization of the prepared monomers (*MP2 was obtained from M2 (endo-isomer of M1)).
Polymers 14 05453 sch004
Polymers 14 05453 g004 550
Figure 4. 1H NMR spectra of M6 and the corresponding ROMP polymer from M6 (CDCl3).
Figure 4. 1H NMR spectra of M6 and the corresponding ROMP polymer from M6 (CDCl3).
Polymers 14 05453 g004
Polymers 14 05453 g005 550
Figure 5. The structure of monomer units of MP4 with trans- and cis-double bonds.
Figure 5. The structure of monomer units of MP4 with trans- and cis-double bonds.
Polymers 14 05453 g005
Polymers 14 05453 g006 550
Figure 6. The parts of 1H NMR spectra of the isomeric ROMP polymers obtained from M1: MP1 (red curve) and MP7 (blue curve).
Figure 6. The parts of 1H NMR spectra of the isomeric ROMP polymers obtained from M1: MP1 (red curve) and MP7 (blue curve).
Polymers 14 05453 g006
Polymers 14 05453 g007 550
Figure 7. The photographs of the powder and thin films of MP3.
Figure 7. The photographs of the powder and thin films of MP3.
Polymers 14 05453 g007
Polymers 14 05453 g008 550
Figure 8. TGA curves for MP1 (a), the enlarged TGA curves for MP1 (b), and TGA curves for MP6 (c).
Figure 8. TGA curves for MP1 (a), the enlarged TGA curves for MP1 (b), and TGA curves for MP6 (c).
Polymers 14 05453 g008
Polymers 14 05453 g009 550
Figure 9. Wide-angle X-ray diffraction (WAXD) patterns for the prepared ROMP polymers.
Figure 9. Wide-angle X-ray diffraction (WAXD) patterns for the prepared ROMP polymers.
Polymers 14 05453 g009
Table
Table 1. The data on the synthesis and some properties of the monomers.
Table 1. The data on the synthesis and some properties of the monomers.
MonomerReaction Conditions aYield, %[α]D b, deg·mL·g−1·dm−1Tm, °C
M1i83−75 (T = 25 °C, CHCl3)86–89
M2i76−125 (T = 20 °C, CHCl3)97–100
M3i72−42 (T = 25 °C, CHCl3)96–98
M4ii68−11 (T = 20 °C, CHCl3)Colorless oil
M5ii71+7 (T = 20 °C, THF)Colorless oil
M6ii54+4 (T = 20 °C, CHCl3)Colorless oil
a: i—three-step procedure, (1) alcohol (4.5 eq.), Et3N, toluene, 55 °C. (2) SOCl2, DMF (few drops), toluene, 90 °C. (3) alcohol (0.9 eq.), pyridine, 90 °C; ii—one-step procedure, alcohol (1.05 eq.), toluene, TsOH, reflux. b: the specific optical rotation was measured at C = 1.
Table
Table 2. ROMP polymerization of diesters of cis-5-norbornene-2,3-dicarboxylic acid over the 2nd generation Grubbs catalyst a.
Table 2. ROMP polymerization of diesters of cis-5-norbornene-2,3-dicarboxylic acid over the 2nd generation Grubbs catalyst a.
PolymerMonomer/[Ru]
Molar Ratio		C, M bYield,
%		Mw × 10−3Mw/Mn cTg, °C d[α]D e,
deg·mL·g−1·dm−1
Polymers 14 05453 i0011000/10.5964882.180−59
Polymers 14 05453 i002750/10.5741901.6136−64
Polymers 14 05453 i003500/10.5944692.1139−34
Polymers 14 05453 i0041000/10.5955822.968−11
Polymers 14 05453 i005500/10.5964572.2−9+10 f
Polymers 14 05453 i006500/10.5922692.2−30+4
a—reaction temperature—+45 °C, solvent—1,2-dichloroethane, [Ru]—the 2nd generation Grubbs catalyst; b—the initial concentration of a monomer; c—the molecular weights of polymers were estimated by means of gel permeation chromatography in THF; d—glass transition temperature according to DSC; e—the specific optical rotation was measured at 22 °C in chloroform solution at C = 1; f—the specific optical rotation was measured in THF solution.
Table
Table 3. Solubility of the ROMP polymers synthesized from diesters of cis-5-norbornene-2,3-dicarboxylic acid a.
Table 3. Solubility of the ROMP polymers synthesized from diesters of cis-5-norbornene-2,3-dicarboxylic acid a.
PolymerCH3CNAcetoneDMADMSOn-HexanePhCH3THFCHCl3
Polymers 14 05453 i007±±±–+±++
Polymers 14 05453 i008–±±–±+++
Polymers 14 05453 i009±±±±±+++
Polymers 14 05453 i010±±±±±+++
Polymers 14 05453 i011–+±±±+++
a—“+”—soluble, “–”—insoluble, and “±”—swelling.
Table
Table 4. Density and fractional free-volume (FFV) for ROMP polymers synthesized from diesters of cis-5-norbornene-2,3-dicarboxylic acid a.
Table 4. Density and fractional free-volume (FFV) for ROMP polymers synthesized from diesters of cis-5-norbornene-2,3-dicarboxylic acid a.
PolymerDensity, g/cm3FFV, %
Polymers 14 05453 i0121.03316
Polymers 14 05453 i0131.06417
Polymers 14 05453 i0141.11013
a—the density of polymer films was determined by the hydrostatic weighing; fractional free-volume was calculated by Bondi’s method [43] from the density of polymer films.
Table
Table 5. The intersegmental and intrasegmental distances (d, Å) evaluated with Bragg-formula for the prepared ROMP polymers.
Table 5. The intersegmental and intrasegmental distances (d, Å) evaluated with Bragg-formula for the prepared ROMP polymers.
Polymer2θ1,°d1, Å2θ2,°d2, Å
MP19.29.617.65.0
MP29.19.717.85.0
MP315.25.8--
MP415.95.6--
MP59.39.517.65.0
MP69.19.719.04.7
Publisher’s Note: MDPI stays neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Share and Cite

MDPI and ACS Style

Nazarov, I.V.; Zarezin, D.P.; Solomatov, I.A.; Danshina, A.A.; Nelyubina, Y.V.; Ilyasov, I.R.; Bermeshev, M.V. Chiral Polymers from Norbornenes Based on Renewable Chemical Feedstocks. Polymers 2022, 14, 5453. https://doi.org/10.3390/polym14245453

AMA Style

Nazarov IV, Zarezin DP, Solomatov IA, Danshina AA, Nelyubina YV, Ilyasov IR, Bermeshev MV. Chiral Polymers from Norbornenes Based on Renewable Chemical Feedstocks. Polymers. 2022; 14(24):5453. https://doi.org/10.3390/polym14245453

Chicago/Turabian Style

Nazarov, Ivan V., Danil P. Zarezin, Ivan A. Solomatov, Anastasya A. Danshina, Yulia V. Nelyubina, Igor R. Ilyasov, and Maxim V. Bermeshev. 2022. "Chiral Polymers from Norbornenes Based on Renewable Chemical Feedstocks" Polymers 14, no. 24: 5453. https://doi.org/10.3390/polym14245453

Note that from the first issue of 2016, this journal uses article numbers instead of page numbers. See further details here.

Article Metrics

Back to TopTop