Laird Rebecca C, Nguyen Nam P, Rusch Sara F, Baltrusaitis Jonas, Macgillivray Leonard R
Department of Chemistry, University of Iowa , Iowa City, Iowa 52242-1294, United States.
PhotoCatalytic Synthesis Group, Faculty of Science and Technology, MESA+ Nanoinstitute, University of Twente , 7500 AE Enschede, The Netherlands.
Cryst Growth Des. 2014 Mar 5;14(3):893-896. doi: 10.1021/cg4016542. Epub 2014 Feb 17.
Though 1,4-disubstituted 1,2,3-triazole rings have been utilized as electronic bridges in the solution phase, the use of a triazole ring to serve as an electronic bridge of small molecules in the crystalline state has been underdeveloped. Here two compounds with a central 1,4-disubstituted 1,2,3-triazole ring are synthesized to investigate the electronic bridging between terminal stilbazole and pyridine groups in the crystalline phase. The electronic properties of the molecules are characterized through solution phase UV-vis spectroscopy, single crystal X-ray diffractions, and density-of-state and gas-phase DFT calculations. We show that the electronic bridging behavior of a 1,4-disubstituted 1,2,3-triazole ring derived from a click reaction is maintained in the solid state by rare head-to-head (hh) packing in noncentrosymmetric crystal environments.
尽管1,4-二取代的1,2,3-三唑环已在溶液相中用作电子桥,但在晶体状态下使用三唑环作为小分子的电子桥的研究仍不充分。在此,合成了两种具有中心1,4-二取代的1,2,3-三唑环的化合物,以研究晶体相中末端二苯乙烯基吡啶和吡啶基团之间的电子桥接。通过溶液相紫外可见光谱、单晶X射线衍射以及态密度和气相密度泛函理论计算对分子的电子性质进行了表征。我们表明,由点击反应衍生的1,4-二取代的1,2,3-三唑环的电子桥接行为通过在非中心对称晶体环境中的罕见头对头(hh)堆积在固态中得以保持。