Kara Yesim S
Kocaeli University, Science and Art Faculty, Department of Chemistry, Umuttepe Campus, 41380 Kocaeli, Turkey.
Spectrochim Acta A Mol Biomol Spectrosc. 2015 Dec 5;151:723-30. doi: 10.1016/j.saa.2015.07.032. Epub 2015 Jul 7.
Eleven novel (3-(substituted phenyl)-cis-4,5-dihydroisoxazole-4,5-diyl)bis(methylene) diacetate derivatives were synthesized in the present study. These dihydroisoxazole derivatives were characterized by IR, (1)H NMR, (13)C NMR and elemental analyses. Their (13)C NMR spectra were measured in Deuterochloroform (CDCl3). The correlation analysis for the substituent-induced chemical shift (SCS) with Hammett substituent constant (σ), inductive substituent constant (σI), different of resonance substituent constants (σR, σR(o)) and Swain-Lupton substituent parameters (F, R) were performed using SSP (single substituent parameter), and DSP (dual substituent parameter) methods, as well as single and multiple regression analysis. From the result of regression analysis, the effect of substituent on the (13)C NMR chemical shifts was explained.
本研究合成了11种新型的(3-(取代苯基)-顺式-4,5-二氢异恶唑-4,5-二亚基)双(亚甲基)二乙酸酯衍生物。这些二氢异恶唑衍生物通过红外光谱、核磁共振氢谱、核磁共振碳谱和元素分析进行了表征。它们的核磁共振碳谱在氘代氯仿(CDCl3)中测定。使用单取代参数(SSP)和双取代参数(DSP)方法以及单变量和多变量回归分析,对取代基诱导的化学位移(SCS)与哈米特取代基常数(σ)、诱导取代基常数(σI)、共振取代基常数的差值(σR、σR(o))以及斯温-卢普顿取代基参数(F、R)进行了相关分析。根据回归分析结果,解释了取代基对核磁共振碳谱化学位移的影响。