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杯[4]吡咯封端的金属卟啉作为阴离子的双位点受体模型。

Calix[4]pyrrole-capped metalloporphyrins as ditopic receptor models for anions.

作者信息

Panda Pradeepta K, Lee Chang-Hee

机构信息

Department of Chemistry, Kangwon National University, Chun-Chon 200-701, Korea.

出版信息

Org Lett. 2004 Mar 4;6(5):671-4. doi: 10.1021/ol0360750.

Abstract

Strapped calix[4]pyrrole-metalloporphyrin conjugates, potential hosts for anionic guests, have been synthesized and characterized. The condensation unexpectedly resulted in the formation of the two conformational isomers of calix[4]pyrrole-capped porphyrins 6 and 7. The anion binding studies revealed that only isomer 6 showed strong binding with fluoride anion in organic solvent, and neither isomer showed any appreciable binding with Cl-, Br-, and I-. [structure: see text]

摘要

已合成并表征了作为阴离子客体潜在主体的束缚杯[4]吡咯 - 金属卟啉共轭物。缩合反应意外地导致形成了杯[4]吡咯封端的卟啉6和7的两种构象异构体。阴离子结合研究表明,仅异构体6在有机溶剂中与氟离子表现出强结合,而两种异构体均未与Cl-、Br-和I-表现出任何明显的结合。[结构:见原文]

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