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作 者:ZHENG Chunying QIU Qiming HAO Liang LI Hui
出 处:《Chemical Research in Chinese Universities》2016年第1期1-7,共7页高等学校化学研究(英文版)
基 金:Supported by the National Natural Science Foundation of China(Nos.21071018, 21271026).
摘 要:Halogen substituted β-amino acids, D,L-3-amino-3-(4-fluoro)phenylpropionic acid(D,L-HL1, 1) and D,L-3-amino-3-(4-bromo)phenylpropionic acid(D,L-HL2, 2), as well as their Cu(II) coordination complexes [Cu(L1)2(CH3OH)2].2CH3OH(3) and [Cu(L2)2(CH3OH)2]-2CHaOH(4) were investigated and their single crystal structures were discussed in details. Supramolecular helical chains were found in β-amino acids 1 and 2 while there was no helix in their coordination complexes 3 and 4. The formation of supramolecular helixes could be due to the hydrogen bonds between terminal -NH3+ and adjacent -COO- in β-amino acids 1 and 2. While, this kind of hydrogen bonds could not be observed in their Cu(II) coordination complexes 3 and 4, in which central-symmetrical dimers could be formed via coplanar coordinated bonds(N-Cu-O) between -NH2 and -COO-.Halogen substituted β-amino acids, D,L-3-amino-3-(4-fluoro)phenylpropionic acid(D,L-HL1, 1) and D,L-3-amino-3-(4-bromo)phenylpropionic acid(D,L-HL2, 2), as well as their Cu(II) coordination complexes [Cu(L1)2(CH3OH)2].2CH3OH(3) and [Cu(L2)2(CH3OH)2]-2CHaOH(4) were investigated and their single crystal structures were discussed in details. Supramolecular helical chains were found in β-amino acids 1 and 2 while there was no helix in their coordination complexes 3 and 4. The formation of supramolecular helixes could be due to the hydrogen bonds between terminal -NH3+ and adjacent -COO- in β-amino acids 1 and 2. While, this kind of hydrogen bonds could not be observed in their Cu(II) coordination complexes 3 and 4, in which central-symmetrical dimers could be formed via coplanar coordinated bonds(N-Cu-O) between -NH2 and -COO-.
关 键 词:β-Amino acid Copper H-BONDING HALOGEN Crystal structure
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