28557-00-8Relevant articles and documents
A One-Dimensional π–d Conjugated Coordination Polymer for Sodium Storage with Catalytic Activity in Negishi Coupling
Chen, Yuan,Tang, Mi,Wu, Yanchao,Su, Xiaozhi,Li, Xiang,Xu, Shuaifei,Zhuo, Shuming,Ma, Jing,Yuan, Daqiang,Wang, Chengliang,Hu, Wenping
, p. 14731 - 14739 (2019)
π-d Conjugated coordination polymers (CCPs) have attracted much attention for various applications, although the chemical states and structures of many CCPs are still blurry. Now, a one-dimensional (1D) π-d conjugated coordination polymer for high performance sodium-ion batteries is presented. The chemical states of the obtained coordination polymer are clearly revealed. The electrochemical process undergoes a three-electron reaction and the structure transforms from C=N double bonds and NiII to C?N single bonds and NiI, respectively. Our unintentional experiments provided visual confirmation of NiI. The existence of NiI was further corroborated by its X-ray absorption near-edge structure (XANES) and its catalytic activity in Negishi cross-coupling.
Asymmetric Synthesis of Chiral Bicyclo[2.2.1]hepta-2,5-diene Ligands through Rhodium-Catalyzed Asymmetric Arylative Bis-cyclization of a 1,6-Enyne
Chen, Chen,Hayashi, Tamio,Meng, He,Ming, Jialin,Sun, Chao,Wei, Haili
supporting information, p. 6311 - 6315 (2021/09/02)
A series of novel chiral diene ligands (1R,4S)-L1, which are based on the bicyclo[2.2.1]heptadiene skeleton and are substituted with methyl and an ester group at the bridgehead carbons, were synthesized through rhodium-catalyzed asymmetric arylative bis-c
Ni-Catalyzed C(sp3)–O Arylation of α-Hydroxy Esters
Monteith, John J.,Rousseaux, Sophie A. L.
supporting information, p. 9485 - 9489 (2021/12/09)
A Negishi cross-coupling of α-hydroxy ester derivatives and arylzinc reagents has been developed. This reaction tolerates both primary and secondary C(sp3)–O alcohol precursors and achieves efficient cross-coupling under Ni catalysis without the need for added external metal reductant, photocatalyst, or additives. The arylation of readily accessible C(sp3)–O electrophiles in this operationally simple, rapid, and mild reaction provides a complementary way of accessing desirable α-aryl ester products.
