Terpyridine and 2,6-di(1H-pyrazol-1-yl)pyridine substituted cyclotri- and polyphosphazene ruthenium(II) complexes: Chemical and physical behaviour

被引:16
作者
Davidson, Ross J. [1 ]
Ainscough, Eric W. [1 ]
Brodie, Andrew M. [1 ]
Jameson, Geoffrey B. [1 ]
Waterland, Mark R. [1 ]
Allcock, Harry R. [2 ]
Hindenlang, Mark D. [2 ]
机构
[1] Massey Univ, Chem Inst Fundamental Sci, Palmerston North 4442, New Zealand
[2] Penn State Univ, Dept Chem, University Pk, PA 16802 USA
关键词
Phosphazene; Polymer; Ruthenium(II) complex; X-ray crystallography; DFT calculations; SMALL-MOLECULE; IRON(II); COPOLYMERS; LIGANDS; PHOSPHAZENE; PRECURSORS; SOLVATE;
D O I
10.1016/j.poly.2014.08.060
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The synthesis of a series of cyclotriphosphazene and polyphosphazene ruthenium(II) compounds is reported using 2,2 ':6 ',2 ''-terpyridine (terpy) and 2,6-di(1H-pyrazol-1-yl)pyridine (bpp) pendant ligands. X-ray crystallography, UV-Vis and resonance Raman spectroscopy have been employed to gain an insight into the physical and coordination behaviour of these complexes and indicate that both the small molecule and their polymeric analogues contain coordinated Ru in an octahedral 'N-6' environment. The results reveal a difference between the chemistry of the ruthenium(II)-bpp-terpy and ruthenium(II)-bis-terpy complexes and demonstrate a means of grafting functional groups to a polyphosphazene backbone under mild conditions. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:429 / 436
页数:8
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