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Chinese Academy of Sciences Institutional Repositories Grid
Mono-, Tetra- and octanuclear transition metal complexes of in situ generated schiff base ligands containing up to 12 coordinating atoms: syntheses, structures and magnetism

文献类型:期刊论文

作者Ding, Cai-Xia1,2; Ni, Jia3; Yang, Yu-Hua1,2; Ng, Seik-Weng4,5; Wang, Bing-Wu6; Xie, Yong-Shu1,2
刊名CRYSTENGCOMM
出版日期2012
卷号14期号:21页码:7312-7319
ISSN号1466-8033
DOI10.1039/c2ce25966d
英文摘要By the reaction of an alkoxyl containing tetraamine, 1,3-bis[(2-aminoethyl)amino]-2-propanol,with various aldehydes, O-vanillin and 2,6-diformyl-4-cresol, in the presence of various metal cations, four novel complexes were synthesized and structurally characterized. Complexes [CoHL1](ClO4)center dot 2MeOH (1) and [NiH2L2](ClO4)(2)center dot 0.5MeOH (2) have mononuclear structures, with the linear di-Schiff base ligand (HL1)(2-) and mono-Schiff base ligand H2L2 generated from in situ reactions under various pH conditions. In complexes [Ni4L3(SCN)(3)(MeOH)]Cl center dot 2.5MeOH (3), and [Cu-8(H2L3)(2)(OH)(4)(ClO4)](SCN)(6)(ClO4)center dot 8H(2)O (4), an interesting 32-membered dodecadentate macrocyclic ligand H4L3 comprising four Schiff base C=N double bonds was generated by a "2+2" type condensation reaction between the tetraamine and the dialdehyde. Complex 3 has a tetranuclear Ni-4 coordination structure with all 12 coordinating atoms of (L-3)(4-) utilized for coordination, and the alkoxyl groups are deprotonated and coordinated in a bridging mode. Complex 4 exhibits an octanuclear Cu-8 coordination structure, with a ClO4- bridging two tetranuclear [Cu4H2L3(OH)(2)](4+) moieties through four weak axial Cu-O coordination bonds. In complex 4, only 10 coordinating atoms of (L-3)(4-) are utilized for coordination, with the two alkoxyl groups left neutral and noncoordinated. It is noteworthy that H4L3 has two long saturated chains in the molecule. Therefore, it has good flexibility and tends to have a nonplanar structure. Variable temperature magnetic data for 3 and 4 indicated the existence of antiferromagnetic interactions, which were discussed based on the structural results.
语种英语
WOS记录号WOS:000309414300037
出版者ROYAL SOC CHEMISTRY
源URL[http://ir.iccas.ac.cn/handle/121111/49223]  
专题中国科学院化学研究所
通讯作者Xie, Yong-Shu
作者单位1.E China Univ Sci & Technol, Key Lab Adv Mat, Shanghai 200237, Peoples R China
2.E China Univ Sci & Technol, Inst Fine Chem, Shanghai 200237, Peoples R China
3.Shantou Univ, Dept Chem, Shantou 515063, Peoples R China
4.Univ Malaya, Dept Chem, Kuala Lumpur 50603, Malaysia
5.King Abdulaziz Univ, Fac Sci, Dept Chem, Jeddah, Saudi Arabia
6.Peking Univ, Beijing Natl Lab Mol Sci, State Key Lab Rare Earth Mat Chem & Applicat, Coll Chem & Mol Engn, Beijing 100871, Peoples R China
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GB/T 7714
Ding, Cai-Xia,Ni, Jia,Yang, Yu-Hua,et al. Mono-, Tetra- and octanuclear transition metal complexes of in situ generated schiff base ligands containing up to 12 coordinating atoms: syntheses, structures and magnetism[J]. CRYSTENGCOMM,2012,14(21):7312-7319.
APA Ding, Cai-Xia,Ni, Jia,Yang, Yu-Hua,Ng, Seik-Weng,Wang, Bing-Wu,&Xie, Yong-Shu.(2012).Mono-, Tetra- and octanuclear transition metal complexes of in situ generated schiff base ligands containing up to 12 coordinating atoms: syntheses, structures and magnetism.CRYSTENGCOMM,14(21),7312-7319.
MLA Ding, Cai-Xia,et al."Mono-, Tetra- and octanuclear transition metal complexes of in situ generated schiff base ligands containing up to 12 coordinating atoms: syntheses, structures and magnetism".CRYSTENGCOMM 14.21(2012):7312-7319.

入库方式: OAI收割

来源:化学研究所

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