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Synthesis and characterization of a chiral Schiff base containing alpha-D-altropyranoside unit and its zinc(II) complex

机译:含α-D-降冰片糖苷单元的手性席夫碱及其锌(II)配合物的合成与表征

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摘要

A novel chiral Schiff base containing alpha-D-altropyranoside unit, methyl 4,6-O-benzylidene-3-deoxy-3-(2-salicylideneaminoethylamino)- alpha-D-altropyranoside (3, Me-Alt-NNOH), has been prepared. Treatment of zinc chloride with 3 in the presence of triethylamine afforded a five-coordinated zinc(II) complex [Zn(Me-Alt-NNO)Cl] (4). Both 3 and 4 have been characterized by infrared, H-1 NMR, C-13 NMR, MS, and elemental analysis. The crystal structure of 4 has been determined by X-ray diffraction. Crystal structure analysis shows that the complex 4 exits a distorted triangular bipyramid geometry and the Schiff base motif acts as a uninegatively charged tetradentate chelating agent. The methoxy and amino groups cis-chelate to the zinc atom and the pyrano-ring is in an ideal C-4(1) chair conformation.
机译:一种新型的手性席夫碱,含有α-D-阿托吡喃糖苷单元,甲基4,6-O-亚苄基-3-脱氧-3-(2-水杨基亚氨基乙基氨基)-α-D-阿托吡喃糖苷(3,Me-Alt-NNOH)准备好了。在三乙胺的存在下用3处理氯化锌,得到五配位的锌(II)络合物[Zn(Me-Alt-NNO)Cl](4)。 3和4均通过红外,1 H NMR,C-13 NMR,MS和元素分析进行​​了表征。 4的晶体结构已经通过X射线衍射确定。晶体结构分析表明,配合物4存在扭曲的三角双锥几何形状,并且席夫碱基序充当带负电荷的四齿螯合剂。甲氧基和氨基与锌原子顺式螯合,吡喃环呈理想的C-4(1)构象。

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