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Synthesis and structures of thienyl-substituted 5-dipyrromethane isomers

机译:噻吩基取代的5-二吡咯甲烷异构体的合成与结构

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The compounds 5(2-thienyl)-and 5(3-thienyl)-dipyrromethane (1 and2, respectively) have been synthesized and isolated from the acid-catalyzed reaction between thiophenes-carboxaldehyde and pyrrole. Characterization by X-ray diffraction confirms molecular structures involving twoortho-substituted pyrrolyl and one thienyl groups. Both the compounds1 and2 were crystallized in the monoclinic space groupP2(1) with cell parametersa = 5.7149(16) angstrom, b = 17.338(6) angstrom, and c = 11.785(4) angstrom, beta = 98.466(9)degrees,V = 1155.0(6) angstrom(3) for compound1; and a = 5.828(4) angstrom, b = 17.424(10) angstrom, c = 11.822(8) angstrom, beta = 98.10(2)degrees, and V = 1188.4(13) angstrom(3) for compound 2.
机译:化合物5(2-噻吩基)-和5(3-噻吩基)-二吡咯甲烷(分别为1和2)已合成并从噻吩-甲醛与吡咯之间的酸催化反应中分离出来。通过X射线衍射表征证实了包含两个邻位取代的吡咯基和一个噻吩基的分子结构。化合物1和2都在单斜空间群P2(1)/ n中结晶,其单元参数为a = 5.7149(16)埃,b = 17.338(6)埃,c = 11.785(4)埃,β= 98.466(9)度对于化合物1,V = 1155.0(6)埃(3);化合物2的a = 5.828(4)埃,b = 17.424(10)埃,c = 11.822(8)埃,beta = 98.10(2)度,V = 1188.4(13)埃(3)。

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