Photodimerization of anthracene derivatives in their neat solid state and in solid molecular compounds

被引:32
|
作者
Zouev, I. [1 ]
Cao, Den-Ke [2 ]
Sreevidya, T. V. [1 ]
Telzhensky, M. [1 ]
Botoshansky, M. [1 ]
Kaftory, M. [1 ]
机构
[1] Technion Israel Inst Technol, Schulich Fac Chem, Inst Technol, IL-32000 Haifa, Israel
[2] Nanjing Univ, State Key Lab Coordinat Chem, Inst Coordinat Chem, Nanjing 210093, Peoples R China
来源
CRYSTENGCOMM | 2011年 / 13卷 / 13期
基金
以色列科学基金会;
关键词
TO-SINGLE-CRYSTAL; SUPRAMOLECULAR FRAMEWORK; ACID; TOPOCHEMISTRY; DIMERIZATION;
D O I
10.1039/c0ce00739k
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The Cambridge Crystallographic Data Center provides valuable data for analysis and detection of compounds with potential to undergo photodimerization in the solid-state. Such analysis is presented for anthracene derivatives, and showed that there are many compounds that their packing in the crystal meets the requirement needed for [4 + 4] photodimerization in the solid-state. The crystal structures of various neat acyl anthracenes before and after exposure to UV light are described and the molecular structures of the dimers are compared with those obtained by exposing molecular compounds possessing a light-stable host (1,1,6,6-tetraphenyl-2,4-hexadiyne-1,6-diol) and light-sensitive acyl anthracenes. While exposing neat compounds to UV light causes disintegration of the single crystal, the reaction in the molecular compounds proceeds in a single-crystal to single-crystal mode until a certain rate of conversion, and then disintegrates.
引用
收藏
页码:4376 / 4381
页数:6
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