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吡喃半乳糖苷取代的 - 杂环卡宾钯(II)配合物的合理设计。用于水相中碳 - 碳偶联的稳定高效催化剂。

Rational design of galactopyranoside-substituted -heterocyclic carbene palladium(ii) complexes. Stable and efficient catalyst for C-C coupling in aqueous media.

作者信息

Hobsteter Ariana W, Lo Fiego Marcos J, Silbestri Gustavo F

机构信息

INQUISUR, Departamento de Química, Universidad Nacional del Sur (UNS)-CONICET Av. Alem 1253 B8000CPB Bahía Blanca Argentina

出版信息

RSC Adv. 2024 Jan 4;14(3):1626-1633. doi: 10.1039/d3ra08031e. eCollection 2024 Jan 3.

Abstract

Following a rational design, three novel palladium(ii) complexes bearing galactopyranoside-based -heterocyclic carbene ligands have been synthesized transmetalation of the corresponding Ag(i) complexes. Palladium(ii) complexes have been characterized by NMR, FT-IR and elemental analysis. Catalytic studies, using the Stille and Suzuki-Miyaura cross-coupling reactions as model C-C coupling, reveal that the complexes are active and reusable. The best results in terms of TON values were achieved in aqueous medium using either the deacetylation of the catalyst or the previously deacetylated catalyst. The catalytic condition using deacetylation was more efficient because it avoids an additional deprotection step.

摘要

通过合理设计,通过相应的Ag(i)配合物的金属转移反应合成了三种带有基于吡喃半乳糖苷的-杂环卡宾配体的新型钯(ii)配合物。钯(ii)配合物已通过核磁共振、傅里叶变换红外光谱和元素分析进行了表征。以Stille和Suzuki-Miyaura交叉偶联反应作为模型C-C偶联反应的催化研究表明,这些配合物具有活性且可重复使用。在水介质中,使用催化剂的脱乙酰化或预先脱乙酰化的催化剂,在TON值方面取得了最佳结果。使用脱乙酰化的催化条件更有效,因为它避免了额外的脱保护步骤。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e89b/10765771/eec04be1425a/d3ra08031e-s1.jpg

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