作者:Shuang Ma、Chong Liu、Rafaël J. Sablong、Bart A. J. Noordover、Emiel J. M. Hensen、Rolf A. T. M. van Benthem、Cor E. Koning
DOI:10.1021/acscatal.6b01673
日期:2016.10.7
potassium tert-butoxide (KO-t-Bu), are screened for a low-toxicity route toward (poly)urethane/urea preparation from carbonate/carbamate esters. On the basis of similar kinetics, the catalytically active species for KHMDS, KO-t-Bu, and KOMe is inferred to be the alkoxide anion RO–, depending on the R group in the carbonate/carbamate. Its activity is much higher than that of TBD. Computational simulation
四种催化剂,即。1,5,7-三氮杂双环[4.4.0]癸-5-烯(TBD),双(三甲基甲硅烷基)酰胺钾(KHMDS),甲醇钾(KOMe)和叔丁醇钾(KO- t- Bu),从碳酸酯/氨基甲酸酯向(聚)氨基甲酸酯/脲制备的低毒途径中筛选了丁烷。根据相似的动力学,推断KHMDS,KO- t- Bu和KOMe的催化活性物质为烷氧基阴离子RO –,具体取决于碳酸盐/氨基甲酸酯中的R基团。它的活性远高于待定。MeO的计算仿真–-已经使用密度泛函理论进行了催化的氨基甲酸酯/脲的形成。计算的活化能与三个的MeO的实验结果接近的比赛-基催化剂。通过缩聚将TBD和KOMe用于无异氰酸酯的聚脲制剂中。再次,KOMe显示出比TBD更高的效率。