Control of molecular architecture by hydrogen bonding: mononuclear versus dinuclear copper(II) complexes with tridentate N2O donor Schiff base isomers

被引：28
作者：
Das, Mithun [1 ]
Chattopadhyay, Shouvik [1 ]
机构：
[1] Jadavpur Univ, Inorgan Sect, Dept Chem, Kolkata 700032, India
来源：
TRANSITION METAL CHEMISTRY | 2013年 / 38卷 / 02期
关键词：
CRYSTAL-STRUCTURES; ANTIBACTERIAL ACTIVITIES; LIGANDS; COORDINATION; DEFINITION;
D O I：
10.1007/s11243-012-9677-1
中图分类号：
O61 [无机化学];
学科分类号：
070301 ; 081704 ;
摘要：
Two isomeric Schiff bases, HL (1) = 1-[(2-dimethylamino-ethylimino)-methyl]-naphthalen-2-ol and HL (2) = 1-[(2-ethylamino-ethylimino)-methyl]-naphthalen-2-ol, have been used to prepare copper(II) complexes in presence of thiocyanate. HL (1) forms a mononuclear complex [Cu(L (1) )NCS] with terminal thiocyanate, whereas the isomeric Schiff base HL (2) , which is capable of hydrogen bonding, gives a dimeric complex, [Cu-2 (L (2) ) (2)(NCS)(2)], with double mu-1,1-NCS bridges. Both complexes are characterized by physico-chemical and spectroscopic methods as well as by single crystal X-ray diffraction studies.
引用
收藏
页码：191 / 197
页数：7
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