Synthesis and Crystal Structure of 1,7-Bis(4-methoxyphenyl)-4-(1,3-dithiolan-2-ylidene)-1,6-heptadiene-3,5-dione

被引:1
作者
Bubbly, S. G. [1 ]
Gudennavar, S. B. [1 ]
Viswam, D. [2 ]
Sudarsanakumar, C. [3 ]
机构
[1] Christ Univ, Dept Phys, Bangalore 560029, Karnataka, India
[2] Sree Narayana Coll, Dept Chem, Cherthala 688524, Kerala, India
[3] Mahatma Gandhi Univ, Sch Pure & Appl Phys, Kottayam 686560, Kerala, India
关键词
Crystal structure; 1,6-Heptadiene-3,5-dione; Curcumin analogue; Ketenedithioacetal; X-ray diffraction; CURCUMINOID ANALOGS; MOLECULAR-STRUCTURE; COPPER-COMPLEXES; ANTIOXIDANT; LONGA;
D O I
10.1007/s10870-010-9859-7
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
The synthesis and crystal structure of 1,7-bis(4-methoxyphenyl)-4-(1,3-dithiolan-2-ylidene)-1,6-heptadiene-3,5-dione is described. This compound crystallizes in the space group P2(1) with unit cell parameters a = 14.207 angstrom, b = 7.752(1) angstrom, c = 19.473(1) angstrom, beta = 91.00(3)degrees, with two molecules in the asymmetric unit. The ketenedithioacetal functionality present between the carbonyl groups prevents the possibility of keto-enol tautomerization in this compound. The cinnamoyl groups are organized parallel to each other due to the push-pull nature of the ketenedithioacetal functionality.
引用
收藏
页码:175 / 179
页数:5
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