Infrared spectra of phthalocyanine and naphthalocyanine in sandwich-type (na)phthalocyaninato and porphyrinato rare earth complexes: Part 12. The infrared characteristics of phthalocyanine in heterol
- 作者：Wei Su ; Meng Bao and Jianzhuang Jiang
- 关键词：Phthalocyanine ; Heteroleptic double-decker ; Infra-red ; Rare earth ; Sandwich
- 刊名：Vibrational Spectroscopy
- 出版年：2005
- 期刊代码：113_09242031
- 类别：ms
- 出版时间：2005
- 卷：39
- 期：2
- 页码：186-190
- 文件大小：199 K
摘要
The infra-red (IR) spectroscopic data for a series of 13 heteroleptic bis(phthalocyaninato) rare earth complexes M(Pc)[Pc(OC8H17)8] [M = Y, Pr, …, Lu except Pm; H2Pc = phthalocyanine; H2Pc(OC8H17)8 = 2,3,9,10,16,17,24,25-octakis(octyloxy)phthalocyanine] have been collected with resolution of 2 cm−1. The IR spectra for M(Pc)[Pc(OC8H17)8] are more complicated than those of homoleptic bis(phthalocyaninato) rare earth counterparts M(Pc)2 and M[Pc(OC8H17)8]2 due to the decreased molecular symmetry of these double-decker compounds, C4v. For this series of heteroleptic bis(phthalocyaninato) rare earth compounds, the Pc
− marker band at 1315–1322 cm−1, attributed to the pyrrole stretching, is found to be dependent on the central rare earth size, shifting slightly to the higher energy along with the decrease of rare earth radius. The coupling of isoindole deformation and aza stretching at 1057–1063 cm−1 and the coupling of pyrrole and aza stretching at 1497–1504 cm−1 are also metal-sensitive. The frequency of the vibration at 880–884 cm−1 is also dependent on the rare earth ionic size. The assignments of the vibration bands for these compounds have been made by comparison with the IR spectra of unsubstituted and in particular the 2,3,9,10,16,17,23,24-octakis(octyloxy)-substituted bis(phthalocyaninato) rare earth analogues M(Pc)2 and M[Pc(OC8H17)8]2.
− marker band at 1315–1322 cm−1, attributed to the pyrrole stretching, is found to be dependent on the central rare earth size, shifting slightly to the higher energy along with the decrease of rare earth radius. The coupling of isoindole deformation and aza stretching at 1057–1063 cm−1 and the coupling of pyrrole and aza stretching at 1497–1504 cm−1 are also metal-sensitive. The frequency of the vibration at 880–884 cm−1 is also dependent on the rare earth ionic size. The assignments of the vibration bands for these compounds have been made by comparison with the IR spectra of unsubstituted and in particular the 2,3,9,10,16,17,23,24-octakis(octyloxy)-substituted bis(phthalocyaninato) rare earth analogues M(Pc)2 and M[Pc(OC8H17)8]2.