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Molecular Chirality and Chiral Superlattice in Crystal of Tetrakis[(pyrrol-1-yl)methyl]methane
引用本文:XU Wei 1**,LU Yin-xiang 1,LIU Chun-ming 1,LAN Bi-jian 1,ZHOU Hui 1 and WANG Jing-mei 2 1. Department of Materials Science,Fudan University,Shanghai 200433,P. R. China, 2. Research Center for Analysis and Measurement,Fudan University,Shanghai 200433,P. R. China. Molecular Chirality and Chiral Superlattice in Crystal of Tetrakis[(pyrrol-1-yl)methyl]methane[J]. 高等学校化学研究, 2004, 20(6): 778-780
作者姓名:XU Wei 1**  LU Yin-xiang 1  LIU Chun-ming 1  LAN Bi-jian 1  ZHOU Hui 1 and WANG Jing-mei 2 1. Department of Materials Science  Fudan University  Shanghai 200433  P. R. China   2. Research Center for Analysis and Measurement  Fudan University  Shanghai 200433  P. R. China
作者单位:XU Wei 1**,LU Yin-xiang 1,LIU Chun-ming 1,LAN Bi-jian 1,ZHOU Hui 1 and WANG Jing-mei 2 1. Department of Materials Science,Fudan University,Shanghai 200433,P. R. China; 2. Research Center for Analysis and Measurement,Fudan University,Shanghai 200433,P. R. China
基金项目:国家自然科学基金,上海市科委资助项目
摘    要:The crystal structure of tetrakis[(pyrrol-1-yl)methyl]methane was determined by X-ray diffraction measurement, and the result shows that it belongs to monoclinic crystal system, space group is P21/n, with a=0.9284(3) nm, b=1.0950(6) nm, c=1.8749(8) nm; α=γ= 90.00(4)°, β=103.63(3)°, V=1.8523(14) nm3, Z=4, ρcalcd.=1.192 kg/m3, μ=0.072 nm-1, F(000)=712, R1=0.0854, wR2=0.1884. It has been found that the molecules exist in two enantiomeric states. Enantioselective self-assemblies such as one-dimensional molecular stacks in a single handedness, homochiral monolayers and a chiral superlattice are specified in this racemic crystal. In addition, a simple technique is advocated to distinguish chiral states from tetrahedral molecules in the solid state. The present R/S nomenclature of the tetracooradinated carbon centers is used solely for its convenience to distinguish the two enantiomeric states, but not used to determine the absolute configurations.

关 键 词:分子 手性特征 手性超点阵 四(吡咯基甲基)甲烷 外消旋晶体 对映选择性自组装
收稿时间:2003-09-08

Molecular Chirality and Chiral Superlattice in Crystal of Tetrakis[(pyrrol-1-yl)methyl]methane
XU Wei,LU Yin-Xiang,LIU Chun-ming,LAN Bi-jian,ZHOU Hui,WANG Jing-mei. Molecular Chirality and Chiral Superlattice in Crystal of Tetrakis[(pyrrol-1-yl)methyl]methane[J]. Chemical Research in Chinese University, 2004, 20(6): 778-780
Authors:XU Wei  LU Yin-Xiang  LIU Chun-ming  LAN Bi-jian  ZHOU Hui  WANG Jing-mei
Affiliation:1. Department of Materials Science, Fudan University, Shanghai 200433, P. R. China;
2. Research Center for Analysis and Measurement, Fudan University, Shanghai 200433, P. R. China
Abstract:The crystal structure of tetrakis[(pyrrol-1-yl)methyl]methane was determined by X-ray diffraction measurement, and the result shows that it belongs to monoclinic crystal system, space group is P21/n, with a=0.9284(3) nm, b=1.0950(6) nm, c=1.8749(8) nm; α=γ= 90.00(4)°, β=103.63(3)°, V=1.8523(14) nm3, Z=4, ρcalcd.=1.192 kg/m3, μ=0.072 nm-1, F(000)=712, R1=0.0854, wR2=0.1884. It has been found that the molecules exist in two enantiomeric states. Enantioselective self-assemblies such as one-dimensional molecular stacks in a single handedness, homochiral monolayers and a chiral superlattice are specified in this racemic crystal. In addition, a simple technique is advocated to distinguish chiral states from tetrahedral molecules in the solid state. The present R/S nomenclature of the tetracooradinated carbon centers is used solely for its convenience to distinguish the two enantiomeric states, but not used to determine the absolute configurations.
Keywords:Achiral molecule  Racemic crystal  Central chirality  Enantioselective self-assembly  Chiral superlattice
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