Condensation Reaction of 1,2,3,4-Tetrahydro-1,10-phenanthroline and Formaldehyde: Synthesis and Crystal Structures of Bis(1,2,3,4-tetrahydro-1,10-phenanthroline-6-yl)methane and Its p-Toluenesulfonate Salt

被引:0
|
作者
Xiaofeng, J. S. [1 ]
Yi, H. P. [1 ]
Mo, Z. L. [1 ]
Chen, S. P. [1 ]
机构
[1] Guilin Univ Technol, Coll Mat Sci & Engn, Guilin, Peoples R China
关键词
1,2,3,4-TETRAHYDRO DERIVATIVES; 1,10-PHENANTHROLINE; HYDROGENATION; QUINOLINES; REDUCTION; CATALYST; CARDANOL;
D O I
10.1134/S1063774517070343
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
A new heterocyclic compound, bis(1,2,3,4-tetrahydro-1,10-phenanthroline-6-yl) methane (1), was obtained by the condensation reaction of 1,2,3,4-tetrahydro-1,10-phenanthroline (tphen) and formaldehyde (HCHO). The p-toluenesulfonate salt of 1, (ptsa)(2) center dot (1H(2)) (2, ptsaH = p-toluenesulfonic acid), is also synthesized and characterized. Cystal structures of 1 and 2 are determined by X-ray single crystal diffraction. The molecules of 1 form a 1D helix supramolecular chain by weak N-H center dot center dot center dot N hydrogen bonds, while in crystal 2, the 1H(2)(2+) cations and ptsa(-) anions are alternately connected by strong N-H center dot center dot center dot O hydrogen bonds and generate a 1D zigzag supramolecular chain. The result also proves that the condensation reaction of tphen can provide its C6 condensation product with high regioselectivity.
引用
收藏
页码:1128 / 1134
页数:7
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