Synthesis, crystallographic and spectral studies of homochiral cobalt(II) and nickel(II) complexes of a new terpyridylaminoacid ligand

被引:10
作者
Wang, Xing [1 ]
Gao, Chang-Qing [2 ]
Gao, Zhi-Yang [1 ]
Wu, Ben-Lai [1 ]
Niu, Yun-Yin [1 ]
机构
[1] Zhengzhou Univ, Coll Chem & Mol Engn, Zhengzhou 450052, Henan, Peoples R China
[2] Henan Acad Arts & Crafts, Zhengzhou 450008, Henan, Peoples R China
基金
中国国家自然科学基金;
关键词
Terpyridylaminoacid ligand; Homochiral supramolecular frameworks; Cobalt and nickel complexes; Characterizations; METAL-ORGANIC FRAMEWORKS; ENANTIOSELECTIVE SEPARATION; CRYSTAL-STRUCTURE; AMINO-ACID;
D O I
10.1016/j.molstruc.2017.12.058
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Based on a chiral terpyridylaminoacid ligand, a series of homochiral Co(II) and Ni(II) complexes, namely, [Co(H2L)(HL)]center dot Cl center dot(PF6)(2)center dot 2H(2)O (1), [Ni(H2L)(HL)]center dot Cl center dot(PF6)(2) (2), [Co-2(L)(2)(CH3OH)(H2O)center dot(PF6)(2)center dot CH3OH (3), [Ni-2(L)(2)(CH3OH)(2)]center dot(PF6)(2)center dot 2CH(3)OH (4), [Co-2(L)(2)(N-3)(2)]center dot 3H(2)O (5), and [Ni-2(L)(2)(SCN)(2)]center dot 4H(2)O (6) have been successfully synthesized and characterized by elemental analysis, TGA, spectroscopic methods (IR, CD and electronic absorption spectra) and single-crystal X-ray diffraction structural analysis (HL = (S)-2-((4-([2,2':6',2 ''-terpyridin]-4'-yl)benzyl)amino)-4-methylpentanoic acid). In the acidic reaction conditions, one protonated (H2L)(+) and one zwitterionic HL only used their terpyridyl groups to chelate one metal ion Co(II) or Ni(II), forming chiral mononuclear cationic complexes 1 or 2. But in the basic and hydro(solvo) thermal reaction conditions, deprotonated ligands (L)(-) acting as bridges used their terpyridyl and amino acid groups to link with two Co(II) or Ni(II) ions, fabricating chiral dinuclear metallocyclic complexes 3-6. Those chiral mononuclear and dinuclear complexes whose chirality originates in the homochiral ligand HL further self-assemble into higher-dimensional homochiral supramolecular frameworks through intermolecular hydrogen-bonding and pi center dot center dot center dot pi interactions. Notably, the coordination mode, hydrogen-bonding site, and existence form of HL ligand can be controlled by the protonation of its amino group, and the architectural diversity of those supramolecular frameworks is adjusted by pH and counter anions. Very interestingly, the 3D porous supramolecular frameworks built up from the huge chiral mononuclear cationic complexes 1 and 2 have novel helical layers only formed through every right-handed helical chain intertwining with two adjacent same helical chains, and the 2D supramolecular helicate 5 consists of two types of left-handed helical chains. (C) 2017 Elsevier B.V. All rights reserved.
引用
收藏
页码:355 / 363
页数:9
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