Chromophoric dipyrrin complexes capable of binding to TiO2: Synthesis, structure and spectroscopy

被引:75
作者
Hall, Jeremy D. [1 ]
McLean, Tracey M. [1 ]
Smalley, Serena J. [1 ]
Waterland, Mark R. [1 ]
Telfer, Shane G. [1 ]
机构
[1] Massey Univ, Inst Fundamental Sci, MacDiarmid Inst Adv Mat & Nanotechnol, Palmerston North, New Zealand
关键词
EXCITED-STATE DYNAMICS; NANOPARTICULATE TIO2; CHARGE SEPARATION; BODIPY DYES; RAMAN; HYDROGEN; METALLOTECTONS; COBALT(III); PORPHYRINS; ADSORPTION;
D O I
10.1039/b912332f
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
The synthesis, characterisation, and TiO2 binding studies of a series of chromophoric complexes of 5-(4-carboxyphenyl)-4,6-dipyrrin (L-b) are presented. The synthesis of [Ru(bipy)(L-b)(2)] (bipy = 2,2'-bipyridine), [Rh(L-b)(3)], and [Pd(L-b)(2)] was achieved by initial coordination of 5-(4-methoxycarbonylphenyl)-4,6-dipyrrin (L-a) followed by hydrolysis of the ester group. The carboxyl groups that are located on the peripheries of these complexes are able to engage in intermolecular hydrogen bonding interactions in the solid state, as revealed by X-ray crystallography. These groups also allow the complexes to anchor to the surface of TiO2 nanoparticles, as evidenced by colouration of the TiO2 and FT-IR spectroscopy. The ability of these complexes to capture a significant fraction of sunlight and to adhere to TiO2 surfaces renders them viable dyes for photochemical devices such as dye sensitised solar cells.
引用
收藏
页码:437 / 445
页数:9
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