Oligomeric (Salen)Mn(III) Complexes Featuring Tartrate Linkers Immobilized over Layered Double Hydroxide for Catalytically Asymmetric Epoxidation of Unfunctionalized Olefins

A series of oligomeric (salen)Mn(III) complexes featuring tartrate linkers were prepared and immobilized over layered double hydroxide, and then used as catalysts for asymmetric epoxidation of unfunctionalized olefins. Comprehensive characterizations including 1H NMR, FT-IR, UV-Vis, elemental analysis, GPC, and ICP-AES were used to illustrate structures of oligomeric (salen)Mn(III) complexes, while powdered XRD, nitrogen physisorption, together with XPS studies provided further details to detect structures of heterogeneous catalysts. Interestingly, scanning electron microscopy found an interesting morphology change during modification of layered supporting material. Catalytic experiments indicated that configuration of major epoxide products was determined by salen chirality more than that of tartrate linker, but enantioselectivity (e.e. values) could be enhanced when tartrate and salen showed identical chiral configurations. Furthermore, the (R,R)-salen moieties linked with (R,R)-tartrate spacers usually offered higher enantioselectivity compared to other combinations. Lastly, Zn(II)/Al(III) layered double hydroxide played as a rigid supporting material in catalysis, showing positive chiral induction and high recycling potential in catalytic reactions.


Introduction
Synthesis of enantiomerically pure epoxides with high efficiency was of great importance and had attracted massive attentions in the fields of pharmaceutical chemistry and material science [1]. The design of efficient and effective catalysts was significant in the asymmetric epoxidation of alkenes to achieve high synthetic availability, optical purity, and atom economy, while addressing corresponding environmental concerns would give more opportunities to industrialization [2,3].
In this regard, Sharpless and co-workers established a Ti(IV)/tartrate system that afforded high enantioselectivities in asymmetric epoxidation of functionalized alkenes like allylic alcohols [4].
Later, chiral (salen)Mn(III) complexes were developed by Jacobsen [5] and Katsuki [6] as highly efficient epoxidation catalysts for transformations of unfunctionalized alkenes [5,6]. The synthetic convenience and environmental friendliness of this system aroused wide interests, and meanwhile, their high epoxidation activity and chiral induction in transformation of cis-, cyclic, and tri-substituted alkenes attracted more intentions for industrialization [7]. In addition, (salen)Mn(III) homogeneous catalysts (complexes) showed little credits in recycling that eventually hampered the road to industrial application [7]. On the basis of above progresses, it seemed highly significant to detect catalytic epoxidation activity of the combination of Ti(IV)/tartrate system with (salen)Mn(III) complex, which may integrate the benefits of two sources and bring about some encouraging results.
On the other hand, to address the environmental concerns and the economic considerations, modification of (salen)Mn(III) complexes to create heterogeneous catalysts was the key for recovery and reuse of catalyst. Therefore, many experiments leading to heterogenization of (salen)Mn(III) complexes were performed, including immobilization of (salen)Mn(III) monomers into Y zeolite [8], grafting of (salen)Mn(III) to polymers through covalent linkage [9], fixation of (salen)Mn(III) monomers onto porous solids through noncovalent linkages [10], as well as mixing (salen)Mn(III) into ionic liquids [11]. Overall, although various immobilizing strategies and many supporting materials had been applied during this process, the endeavors carried out so far have not been so successful, particularly regarding poor fresh catalysis or gradually declining recycling outputs. In practice, accessibility of substrate to metal center was usually limited by supporting materials [12], whose weak solubility in solvents led to leaching of active components from catalysts, which not only depressed recycling catalysis, but also contaminated products [12]. Therefore, it can be seen that developing new and effective supporting materials still deserves more endeavors.
In recent years, the employment of new supporting materials, particularly those bearing a highly ordered structure, appeared to be a really promising strategy to construct heterogeneous (salen)Mn(III) catalysts. Herein, the highly ordered structure may provide a large amount of uniform catalytic microenvironments for transformation along with high chemoselectivity and stereoselectivity [13]. Among these candidates, layered double hydroxide (LDH), for instance, a stable layered material facilitating an experimental composition of [M 2+ 1-x M 3+ x (OH) 2 ][A n-] x/n ·zH 2 O, had aroused increasing attentions owing to their various applications in industry, including removal of chlorinated compounds from aqueous solution [14], adsorption and decontamination of radioactive elements [15], reduction of flammability [16], electrical applications [17], or catalysis [18]. Overall, owing to synthetic availability and low cost of LDH materials, applications of LDH would become more and more attractive in many fields.
In structural respects, the layers of LDH were bound together by van der Waals or electrostatic interactions, so interlayer spaces of LDH could be used through exfoliation or intercalation, which eventually made LDH a particularly attractive supporting material for creating various composites [19]. A sulphonato-(salen)Mn(III) was intercalated into Zn(II) and Mg(II)/Al(III) LDH by Anderson [20] and Choudary [21], in order to construct efficient epoxidation catalysts, indicating interlayer spaces of LDH were flexible enough to accommodate larger molecules. Furthermore, Wypych and co-workers also proved hydroxyl groups on LDH surfaces could be modified by (3-aminopropyl)triethoxysilane to support porphyrin complexes, further broadening applications of LDH [22]. At the same time, LDH materials showed obvious structural memory effects in pollutant adsorption applications [23], which may also improve catalyst endurance and play a key role in catalyst recycling.
On the basis of the above progresses, four chiral (salen-tartrate)Mn(III) polymer complexes as well as one (salen)Mn(III) monomer complex were synthesized in this work and then applied into catalytic asymmetric epoxidation of alkenes ( Figure 1). This part of the research was carried out in order to detect the possible synergistic effects of multiple chiral centers within one polymer complex over catalytic epoxidation reactions. Furthermore, a Zn(II)/Al(III) layered double hydroxide was prepared and then aminated for hosting (salen-tartrate)Mn(III) polymers through axial coordination, which were further used as catalysts for asymmetric epoxidation. In addition to the abovementioned advantages of LDH using as a catalyst, amination of LDH would give many coordination ligands for supporting (salen-tartrate)Mn(III) polymers, which not only seemed more rigid and endurable than other physically adsorbed immobilizations, but also fixed multiple chiral centers in order in support of accomplishing high chiral induction in catalysis. All in all, this work would contribute to heterogeneous asymmetric catalysis and corresponding materials science.

Synthesis of Chiral Ligands (Compound L, Scheme 1)
(R,R)-1,2-diammoniumcyclohexane mono-(+)-tartrate salt (0.45 g, 1.7 mmol), anhydrous K 2 CO 3 (0.47 g, 3.4 mmol), and distilled water (15 mL) were mixed into a round-bottomed flask (250 mL) at room temperature. Then, dry ethanol (6 mL) was introduced under magnetic stirring. The resulting cloudy solution was heated at 75 • C for 2 h under stirring, and then cooled to room temperature. Next, this solution was extracted by CH 2 Cl 2 (4 × 5 mL) to obtain free diamine (Compound 4a, Scheme 1). The CH 2 Cl 2 phase was then slowly added to a pre-prepared ethanol solution of compound 3a (0.9 g, 1.7 mmol, in 20 mL, Scheme 1) at room temperature under stirring. The orange solution was refluxed at 80 • C for 3 h, whose solvent was evaporated under reduced pressure. The crude product thus obtained was dissolved in CH 2 Cl 2 (30 mL), the organic layer was washed with distilled water (50 mL), brine (50 mL), dried over anhydrous Na 2 SO 4 , and then filtered. Solvent was removed by using rotary evaporation, and Compound L1 was obtained as yellow sticky solid (0.96 g). 1        by ICP-AES. Mnx@aL (x = 2, 3, 4) were prepared according to the same process (Section S4, Supplementary data).

Design and Synthesis of Catalysts
Design of the present catalysts was a rational combination of different chiral sources for one conversion target.
Once Land D-tartrate were combined with (R,R)-or (S,S)-1,2-diammoniumcyclohexane, four resulting polymer complex catalysts (Mnx, x = 1, 2, 3, 4) should have short-range ordering. Herein, the monomer Mn5, however, appeared as a comparative criteria to illustrate functions of tartrate linkers (Figure 1). Taking into account flexibility of the present four polymer complexes, they were subsequently immobilized over Zn/Al LDH.
The Mnx (x = 1, 2, 3, 4) were synthesized according to the route that is shown in Scheme 1. At first, the connection of 3-tert-butyl-5-chloromethyl-2-hydroxybenzaldehyde (Compound 1, Scheme 1) with sodium tartrate dihydrate (Compound 2, Scheme 1) was realized along with acceptable yields, when triethylamine were selected as base and solvent (Scheme 1). Sensitivity of this kind of transformation (esterification) was determined by the untouched tartrate, and other strong bases including LiOH, NaOH, or K 2 CO 3 would destroy tartrate and were not available in practice. In the meantime, free chiral diamine should be extracted from alkaline solution due to the same reason, before its polymerization with bis-aldehyde (Scheme 1).
Furthermore, due to low cost and synthetic availability, Zn/Al LDH was prepared according to the method shown in Scheme 2. In order to build more linkers on support, Zn/Al LDH was aminated, leaving many amino groups for accommodating (tartrate-salen)Mn(III) polymers, which actually fixed the flexible Mnx (x = 1-4) into a confined environment (Scheme 2).  (Figure 2b). Based on the comparison of Mn1 with L1, the red shift was observed on C=N stretching from 1649 (L1) to 1618 cm −1 (Mn1) (Figure 2a,b), which could be assigned to the coordination of nitrogen to Mn 3+ that reduced electron density on C=N bond [28]. On the other hand, red shift of tartrate from 1772 (L1) to 1741 cm −1 (Mn1) and that of C-O on tartrate from 1559 (L1) to 1544 cm −1 (Mn1) could be attributed to coordination of tartrate part to Mn 3+ (Figure 2a,b), probably leading to a curved configuration of Mn1 more than a linear one.  (Figure 2b,d), revealing degradation of coordination between the tartrate and manganese center, which also indicated Mn1 were flattened at the LDH surface more than being rolled.

UV-Vis Spectroscopy
UV-Vis spectra of L1, Mn1 and Mn1@aL are shown in Figure 3. For L1, the bands that appeared at 292 and 340 nm could both be ascribed to charge transfer transitions of salen ligands (Figure 3a), while Mn1 showed corresponding responses at 291 and 343 nm (Figure 3b), exhibiting two small shifts, probably because of the coordination of manganese [26]. If Mn1 was axially immobilized over amino-LDH, charge transfer transition of salen ligand was shifted to 293 and 335 nm, together with a new ligand-to-metal charge transfer transition that occurred at 428 nm ( Figure 3c). Herein, two shifts (Figure 3b,c) indicated the interaction between Mn1 and amino-LDH, confirming immobilization was effective [26].

Nitrogen Physisorption
Both Zn/Al LDH and Mn1@aL showed a type II isotherm, but Zn/Al LDH had a H3 hysteresis loop, while Mn1@aL did not show an obvious hysteresis loop ( Figure 4) [30]. Therefore, Zn/Al LDH should have a layered structure that represented unrestricted monolayer-multilayer adsorption of nitrogen [30]. Difference on hysteresis loop revealed that Zn/Al LDH were probably an aggregate of plates with slit-shaped pores, but Mn1@aL looked like a non-porous material, corresponding to its flat pore size distribution (Figure 4b'). Back to the way Mn1@aL formed, 3-APTMS supposedly filled in the tiny pores on every plate of Zn/Al LDH through self-assembling [22], and its further coordination with Mn1 led to this result. Naturally, Mn1@aL had a larger pore radius but smaller pore volume and BET surface area than Zn/Al LDH (Table 1).  a Surface area (m 2 g −1 ) determined by BET method based on N 2 adsorption. b Pore volume (cm 3 g −1 ), BJH method on N 2 adsorption. c Pore radius (nm), BJH method on N 2 adsorption. d Bulk density (g cm −3 ). e Crystallite size (nm) based on BET surface area: d S = 6/(S BET ·ρ), ρ bulk density. f Diameter of particle in CH 2 Cl 2 (nm). g Zeta potential of particle in CH 2 Cl 2 (mV). Figure 5 showed powdered XRD spectra of Zn/Al LDH and Mn1@aL. First of all, the present Zn/Al LDH showed a basal spacing of 20.24 Å (2θ = 4.36 • , asterisk, Figure 5a), which is smaller than that of 26.2 Å of Mg-Al LDH [22], but much larger than that of 7.54 Å of Zn-Al LDH (CO 3 2− as anion) [23], indicating both cation and anion affected basal spacing of LDH materials. Furthermore, Zn/Al LDH also showed several broad and flat bands at 2θ = 7.5-55.0 • (Figure 5a), which are different with those found in Zn-Al LDH (CO 3 2− as anion) [23], mainly because benzoate anion has a much poorer crystallinity than carbonate. After immobilization, the sample obtained (Mn1@aL) showed a smaller basal spacing (16.41 Å, 2θ = 5.36 • , asterisk in Figure 5b) than the support (Zn/Al LDH of this work, 20.24 Å), suggesting that many guest molecules were dispersed into layers of LDH through immobilization (Scheme 2). Mn1@aL also showed two sharp diffraction peaks (circles in Figure 5b), which could be ascribed to 200 (2θ = 31.53 • ) and 220 (2θ = 45.19 • ) diffractions of aluminum(II) oxide (AlO) phase (PDF No. 75-0278), probably stemming from the reduction of Al 3+ of Zn-Al-[C 6 H 5 COO] LDH with 3-APTMS during immobilization (Scheme 2). Furthermore, in other regions, the diffraction peaks became wide and flat (Figure 5b), similar to the reported tendency [22,23,31], indicating the poor crystallinity of synthetic sample after immobilization with 3-APTMS (Scheme 2), and the effective immobilization process as well (Scheme 2).

Chemical Composition
Elemental analyses, metal contents, and molar ratio of N to Mn were summarized in Table 2 (Figure 2c) (Figure 2d). However, the higher molar ratio of N/Mn verified that amino groups were excessive so as to saturate all manganese centers.

X-ray Photoelectron Spectroscopy
Binding energy and surface atomic composition of synthetic products were summarized in Table 3. In general, molar ratios of Al to Zn on surfaces of Zn/Al LDH and amino-LDH were both 2.0 (Table 3), but corresponding average values were fixed at 0.33 ( Table 2), revealing that Al 3+ were focused on exterior surface, and Zn 2+ on interiority of LDH layers. Traces of nitrogen on the Zn-Al LDH surface mainly came from starting materials [25], but a higher molar ratio of nitrogen on amino-LDH was derived from coupling of 3-APTMS. Probably due to attachment of Mn1, carbon composition of Mn1@aL increased, but those of Si, N, and Zn declined sharply (Table 3), which suggested amino-LDH were tightly sealed by Mn1. Furthermore, atomic percentage of Mn was 0.4% on the surface of Mn1@aL, but average Mn of Mn1@aL was 0.2% based on its ideal formula, revealing interlayer spaces of Mn1@aL were filled with Mn1, but its content was sparser that that on exterior surfaces.

Scanning Electron Microscopy
Size and morphology of Zn/Al LDH, amino-LDH, and Mn1@aL, were characterized by scanning electron microscopy, as shown in Figure 6. A planar surface could be found in Zn/Al LDH (Figure 6a), but unexpectedly its attachment to 3-APTMS created spheres with diameters ranging from 3 µm to 6 µm (Figure 6b). During immobilization of Mn1, the morphology of the synthetic product changed again, spherical structure collapsed and Mn1@aL was obtained as much smaller particles (Figure 6c).

Study of Catalytic Conditions
First of all, the synthesized catalysts (from Mn1 to Mn4) were quite soluble in many organic solvents including dichloromethane, acetone, diethyl ether, and acetonitrile, while they were less soluble in n-hexane and ethanol, but showed very poor hydrophilicity. Thus, to optimize catalytic conditions, enantioselective epoxidation of styrene was carried out in these solvents at 0 • C by using Mn1 as a catalyst, in which iodobenzene (PhIO) was employed as an oxidant. According to catalytic results that are shown in Table 4, it can be seen that catalytic conversion, enantioselectivity, and turnover frequency were highly affected by the solvent. In practice, Mn1 was almost insoluble in water, which was aggregated and deposited on the wall or bottom of the flask during the reaction, so interaction between Mn1 and substrate at the molecular level seemed to be very poor, and conversion and enantioselectivity were depressed simultaneously (entry 6, Table 4). Another protonic solvent, ethanol, appeared to be inappropriate also, although a slightly improved result was obtained compared to water (entries 5 vs. 6). More promising enantioselectivity and acceptable conversion were derived from the use of non-protonic solvents such as dichloromethane or n-hexane (entries 7 and 4), probably because the non-protonic solvents could promote S N 2 reactions like epoxidation more than S N 1 [32]. Catalyst loading also played a key role in outputs such as conversion and enantioselectivity. Although the highest conversion (26%) was realized by using the largest catalyst loading (6 mol%) among three dichloromethane facilitated reactions (entries 9 vs. 7 and 8), its corresponding e.e. was lower than that found in 3 mol% (entries 7 vs. 9). On the basis of the above experiments, dichloromethane and 3 mol% of catalyst loading were optimized for the following reactions.

Homogeneous Catalysis
The synthesized polymer catalysts (Mn1 to Mn4) were introduced to asymmetric epoxidation of unfunctionalized alkenes such as styrene, α-methylstyrene, trans-stilbene, and indene. The monomer, Mn5, was also selected as comparative criteria in order to observe the roles of tartrate spacers in catalyst activity or chiral induction. As shown in Table 5, all reactions proceeded well and would be accomplished within 6 h under monitoring of TLC (PMA coloration). Furthermore, iodobenzene (PhIO) was a unique oxidant that was almost insoluble in dichloromethane, thus the oxygen transfer occurred slowly on PhIO surface, naturally leading to comparatively higher e.e. values, along with less abundant conversions. This tendency was quite different with those found in mCPBA oxidized epoxidations (entries 2 vs. 1, 8 vs. 7, 14 vs. 13, and 20 vs. 19, Table 5).  Table 4. b Catalyst loading, based on molar ratio of Mn to alkene (3 mol%). c PhIO or mCPBA, 1 mmol. d As in Table 4. e As in Table 4, for styrene oxide [33]. In addition, major epoxide configurations of α-methylstyrene oxide [33], trans-stilbene oxide [33], and indene oxide [34] were determined by chiral HPLC, after comparison with literatures (Section S5, Supplementary data). f As in Table 4.
The Mn1, derived from the linkage of (R,R)-salen with (R,R)-tartrate, provided the best enantioselectivity as well as acceptable conversion in asymmetric epoxidation of styrene (entry 1, Table 5), but its enantiomer Mn4, the combination of (S,S)-salen with (S,S)-tartrate, could not show equal results (entries 5 vs. 1, Table 5). Furthermore, Mn1 showed much better e.e. than Mn2, suggesting enantioselectivity would be improved when both tartrate linker and salen had the same (R,R)-configuration (entries 1 vs. 3, Table 5). In addition, chiral induction of Mn1 looked more prospective than Mn5 too (entries 1 vs. 6, Table 5), further indicating the conjunction of (R,R)-tartrate with (R,R)-salen was advantageous in epoxidation of styrene. In association with the red shift of tartrate that was found in FT-IR spectra of L1 and Mn1 (curves a and b, Figure 2), it can be seen that chiral tartrate should affect chiral induction through its coordination with Mn center. Nevertheless, configuration of major styrene oxides was still determined by chirality of salen (entries 1, 2 to 6, Table 5).
Configurations of major epoxides of α-methylstyrene were maintained in the epoxidations that were catalyzed by Mn1 to Mn5 (entries 7 to 12, Table 5). Furthermore, Mn1, Mn2, and Mn5 showed considerably higher e.e. values and moderate to high conversions for asymmetric epoxidation of α-methylstyrene (entries 7, 9, and 12, Table 5), obviously proposing the dominant role of (R,R)-salen in chiral configuration determination more than tartrate chirality. Next, catalytic activity of Mn2 (entry 9, Table 5), derived from the linkage of (R,R)-salen with (S,S)-tartrate, was comparable to the chiral sugar moiety-modified (salen)Mn(III) system [35], which may emphasize again that the additional chirality would affect chiral induction through coordination with Mn. On the other hand, catalytic epoxidation of indene gave excellent e.e. values, satisfactory conversions, as well as good TOFs, when salen and tartrate were configurationally identical (entries 19 and 23, Table 5). However, neither polymer catalysts (Mn1 to Mn4) nor monomeric Mn5 could increase chiral induction in epoxidation of trans-stilbene, and there are actually no e.e. values higher than 40% that are observed in all experiments (entries 13 to 18, Table 5).
Under homogeneous manner, Mn5 obviously exhibited more advantages than polymer catalysts in epoxidations of α-methylstyrene (entry 12, Table 5) and trans-stilbene (entry 18, Table 5). Mn1 showed comparatively higher e.e. values and acceptable to good conversions for conversions of styrene (entry 1, Table 5), α-methylstyrene (entry 7, Table 5), and indene (entry 19, Table 5). Mn4 gave a nice performance in transformation of indene too, which both emphasized the important role of uniform configuration that distributed between salen and tartrate.

Heterogeneous Catalysis from Zn/Al LDH-Supported (Tartrate-Salen)Mn(III)
Pure Zn/Al LDH and amino-LDH (3 mol% Al on alkene) had been respectively loaded as catalysts in asymmetric epoxidation of styrene, and neither Zn/Al LDH nor amino-LDH could give considerable epoxide products under TLC monitoring for 12 h, which meant (tartrate-salen)Mn(III) were catalytically active centers (entries 1 and 2, Table 6). Other catalytic reactions proceeded smoothly in the presence of either PhIO or mCPBA, but PhIO usually showed better e.e. values than mCPBA for almost all epoxidation reactions except for the case of indene catalyzed by Mn1@aL (entries 28 vs. 27, Table 6), probably due to a non-catalyzed way facilitated by mCPBA for epoxidation of alkenes [36].
Styrene was not an appropriate substrate for Mn1@aL to Mn4@aL, no excellent conversions and e.e. values were simultaneously detected for one single catalytic round (entries 3-10, Table 6), supposedly it was highly relative to a low enantiofacial selectivity in the transition state of catalytic styrene epoxidation [37]. Within this scope, Mn1@aL afforded 88% e.e. (R) and 29% conversion (entry 3, Table 6), while Mn3@aL afforded 69% e.e. (S) with 81% conversion (entry 7, Table 6), probably because the Zn-Al LDH matrix solidified a chiral-inducing environment for these two combinations. Similarly, there were no significant improvements in both conversion and enantioselectivity for epoxidation of trans-stilbene compared with homogeneous results (Table 4), and layered confinement was poor in promoting enantioselectivity (entries 19 to 26, Table 6). Even so, examples of identical chirality like Mn1@aL (entry 19, Table 6) and Mn4@aL (entry 25, Table 6) still showed better results than other endeavors. a Conditions (as in Section 2.2): alkene (1 mmol), ammonium acetate (co-catalyst, 0.12 mmol), CH 2 Cl 2 (5 mL), T (273 K), time (6 h). b Catalyst loading, based on the molar ratio of Mn content to alkene (3 mol%). c PhIO or mCPBA, 1 mmol. d As in Table 3, and data in parentheses represented consecutively recycled results. e No epoxides were found on HPLC. f As in Table 5, and data in parentheses represented consecutively recycled results along with configurations of major epoxides throughout recycling (Section S5, Supplementary data). g Turnover frequency of cycle fresh, h −1 .
Real progresses were found in epoxidation of α-methylstyrene, where Mn4@aL afforded a 97% conversion together with 93% e.e value under PhIO, but recycling failed (entry 17, Table 4). In the meantime, continuous high conversions and stable e.e. values appeared in the recycling catalyzed by Mn1@aL and Mn2@aL (entries 11 and 13, Table 6), being much better than their corresponding homogeneous catalysis (entries 7 and 9, Table 5), which was also equal or comparable to several heterogeneous systems [32,34]. Asymmetric epoxidation of indene succeeded too, when Mn3@aL had been loaded in association with PhIO, where conversions were maintained at a range of 69% to 91%, while e.e. values at 90% to 97%, showed potentials in large-scale production (entry 31, Table 6).
In this section, Mn1@aL looked like a powerful and steady heterogeneous catalyst for most alkenes in enantioselectivity as well as conversion. Mn3@aL should be second, but Mn2@aL and Mn4@aL were modest. Compared with homogeneous results (Table 5), identical chirality of salen and tartrate still offered positive chiral induction at this layered confinement.

Conclusions
A series of novel (tartrate-salen)Mn(III) polymer catalysts were prepared and employed in asymmetric epoxidations of unfunctionalized alkenes under both homogeneous and heterogeneous manners, which revealed chiral synergetic effects of salen chirality with tartrate linker chirality. In addition to comprehensive characterizations of the synthesized intermediates and products, scanning electron microscopy revealed an interesting morphological change during chemical modification of Zn/Al LDH surfaces. Other characterizations including nitrogen physisorption and powdered XRD indicated Mn polymers were dispersed into LDH. On the other hand, when salen unit and tartrate linker showed identical configurations, the enhanced enantioselectivity could be obtained. Herein, Mn1, a combination of (R,R)-tartrate with (R,R)-(salen)Mn(III), along with its heterogeneous catalysts, showed the best catalytic performance involving chiral induction, activity, as well as stability. In addition, α-methylstyrene and indene appeared to be appropriate substrates in this system, but trans-stilbene and styrene showed little credits as substrates.