Hagspiel Stephan, Arrowsmith Merle, Fantuzzi Felipe, Vargas Alfredo, Rempel Anna, Hermann Alexander, Brückner Tobias, Braunschweig Holger
Institute for Inorganic Chemistry, Julius-Maximilians-Universität Würzburg, Am Hubland, 97074, Würzburg, Germany.
Institute for Sustainable Chemistry & Catalysis with Boron, Julius-Maximilians-Universität Würzburg, Am Hubland, 97074, Würzburg, Germany.
Angew Chem Int Ed Engl. 2021 Mar 15;60(12):6446-6450. doi: 10.1002/anie.202015508. Epub 2021 Feb 3.
Reduction of (CAAC)BBr (NCS) (CAAC=cyclic alkyl(amino)carbene) in the presence of a Lewis base L yields tricoordinate (CAAC)LB(NCS) borylenes which undergo reversible E/Z-isomerization. The same reduction in the absence of L yields deep blue, bis(CAAC)-stabilized, boron-doped, aromatic thiazolothiazoles resulting from the dimerization of dicoordinate (CAAC)B(NCS) borylene intermediates.
在路易斯碱L存在的情况下还原(CAAC)BBr (NCS)(CAAC = 环状烷基(氨基)卡宾)会生成三配位的(CAAC)LB(NCS)硼烯,该硼烯会发生可逆的E/Z异构化。在没有L的情况下进行相同的还原反应会生成深蓝色的、由双(CAAC)稳定的、硼掺杂的芳香族噻唑并噻唑,这是由二配位的(CAAC)B(NCS)硼烯中间体二聚而成的。