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一些双取代甲臜的合成及光谱性质

Synthesis and spectral properties of some bis-substituted formazans.

作者信息

Tezcan Habibe

机构信息

Department of Chemistry, Gazi University, Faculty of Gazi Education, Teknikokullar, 06500 Ankara, Turkey.

出版信息

Spectrochim Acta A Mol Biomol Spectrosc. 2008 Mar;69(3):971-9. doi: 10.1016/j.saa.2007.05.061. Epub 2007 Jun 5.

Abstract

Novel, 1,4-bis-[3,3'-phenyl-5,5'-(o-carboxyphenyl)-formaz-1-yl]-benzene-o-sulphonic acid and its derivatives contained OH group at the o-, m-, p-positions of the 3-phenyl ring were synthesized. The structures of the formazans were confirmed by elemental analyses, GC-mass, IR, (1)H NMR, UV-vis spectra. Their absorption properties were investigated. It was seen that lambda(max) values shifted towards shorter wave lengths by 130nm in CSPF relative to 1,3,5-triphenylformazan (TPF) due to the fact that the structure of CSPF contained electron withdrawing COOH and SO(3)H groups (hypsochromic effect). With binding of OH group to 3-phenyl ring of CSPF, it was observed a small bathochromic effect in accordance to the electron donating effect of OH group.

摘要

合成了新型的1,4-双-[3,3'-苯基-5,5'-(邻羧基苯基)-甲臜-1-基]-苯-邻磺酸及其在3-苯基环的邻、间、对位含有羟基的衍生物。通过元素分析、气相色谱-质谱联用、红外光谱、核磁共振氢谱、紫外-可见光谱对甲臜的结构进行了确证。研究了它们的吸收性能。可以看出,由于CSPF的结构中含有吸电子的COOH和SO₃H基团(紫移效应),相对于1,3,5-三苯基甲臜(TPF),CSPF在氯仿-硫酸-磷酸(CSPF)中的最大吸收波长(λmax)值向短波方向移动了130nm。随着羟基与CSPF的3-苯基环结合,根据羟基的供电子效应,观察到了较小的红移效应。

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