Infrared spectroscopic characteristics of mixed rare earth triple-decker complexes with phthalocyaninato and 5-(4-hydroxyphenyl)-10,15,20-tris(4-octyloxy)porphyrinato ligands.
Infrared spectroscopic characteristics of mixed rare earth triple-decker complexes with phthalocyaninato and 5-(4-hydroxyphenyl)-10,15,20-tris(4-octyloxy)porphyrinato ligands.
复制标题
含有酞菁和 5-(4-羟基苯基)-10,15,20-三(4-辛氧基)卟啉配体的混合稀土三层配合物的红外光谱特征。
DOI:
10.1016/j.saa.2012.11.058
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发表时间:
2013
期刊:
影响因子:
--
通讯作者:
Fanli Lu
中科院分区:
文献类型:
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作者:
Wendong Wang;Guihong Bao;Yajun Mao;Fanli Lu
The infrared (IR) spectroscopic data for a series of nine mixed rare earth triple-deckers M2III[TO(OH)PP](Pc)2] [M=La⋯Dy, except Pm, Y and Ho⋯Lu; H2Por=5-(4-hydroxyphenyl)-10,15,20-tris(4-octyloxyphenyl)porphyrin, Pc=unsubstituted phthalocyanine] with tervalent rare earths have been collected. For M2III[TO(OH)PP](Pc)2], typical IR marker bands for the unsubstituted phthalocyanine dianion Pc2−are strong bands at 1327–1329cm−1, and a weak band around 1370–1383cm−1. They can be assigned to pyrrole CC stretchings. The absence of Pc2−another marker IR band around 1376cm−1demonstrates that the cerium metal ion in the IR spectrum of Ce2III[TO(OH)PP](Pc)2] exists as intermediate valence state between III and IV. The IR spectra of these mixed triple-decker complexes reveal that the frequencies of pyrrole stretching, isoindole breathing, and aza stretchings are decreased sensitive to the rare earth ionic size, and remain basically unchanged along with the lanthanide contraction. These facts indicate that the π–π interactions in these mixed triple-deckers are weaker than those in the double-deckers.
DOI:
--
发表时间:
1999
期刊:
影响因子:
--
作者:
P. ArnoldDennis;JiangJianzhuang
通讯作者:
JiangJianzhuang