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Solvothermal Syntheses, Crystal Structures and Catalytic Properties of Four Chiral Compounds Built from (R)-4-(4-(1-Carboxyethoxy)penoxy) Benzoic Acids

机译:由(r)-4-(4-(1-羧乙氧基)甲氧基)苯甲酸建立的四种手性化合物的溶剂热合成,晶体结构和催化特性

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摘要

A series of chiral metal-organic compounds [Ag(cpfa)(phen)] (1), [Ag(cpna)(phen)] (2), [Cu(cpna)(phen)]*2H2O (3), [Cd2(cpna)2 (phen)2]n (4) (H2cpfa=(R)-4-(4-(1-carboxyethoxyphenoxy) phenoxy-3-fluorobenzoic acid; H2cpna=(R)-4-(4-(1-carboxyethoxy) phenoxy)-3-nitrobenzoic acid; phen=1,10-phenanthroline) has been successfully obtained via solvothermal reactions and characterized by IR spectra, elemental analyses, thermo gravimetric analyzer (TGA), solid-state circular dichroism (CD) and powder X-ray diffraction (PXRD). Compounds 1–4 all crystallize in chiral space groups and their CD spectra exhibit obvious positive or negative Cotton effects, indicating their homochirality. Rich hydrogen bonds based on carboxylic groups and π-π interactions between adjacent phen molecules are present in the four compounds. It is also found that the pH value and reactant ratio have an impact on the growth of the compounds. In addition, their asymmetric catalytic activities for Henry reaction have also been investigated.
机译:一系列手性金属有机化合物[Ag(cpfa)(phen)](1),[ag(cpna)(peh)](2),[cu(cpna)(phen)]*2H2O(3),[ CD2(CPNA)2(PEN)2] N(4)(H2CPFA =(R)-4-(4-(1-羧乙氧基)苯氧-3-氟苯甲酸; H2CPNA =(R)-4-(4-(4-(4-)) 1-羧乙氧基)苯氧基-3-硝基苯酸; PEN = 1,10-苯磺烷氨酸)已通过溶剂热反应成功获得,并通过IR光谱,元素分析,Thermo Gravimetric Analyzer(TGA),固态圆形二色症(CD)(CD)(CD) )和粉末X射线衍射(PXRD)。化合物1-4在手性空间群中结晶且CD光谱表现出明显的阳性或负棉作用,表明它们的同型同质性。基于羧基和π-π相互作用的丰富氢键和π-π相互作用相邻的现象分子存在于四种化合物中。还发现pH值和反应物比对化合物的生长有影响。此外,它们的亨利反应的不对称催化活性也是调查。

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