Bispidine coordination chemistry

IF 3.3 3区 化学 Q2 CHEMISTRY, INORGANIC & NUCLEAR Dalton Transactions Pub Date : 2025-01-30 DOI:10.1039/D5DT00050E
Katharina Bleher, Patrick A. Cieslik and Peter Comba
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Abstract

Bispidines are extremely rigid ligands, easy to prepare in a large variety, with denticities of four to ten, various donor sets and charges, for mono- and oligonuclear transition metal, main group and rare earth complexes. In the last approx. 20 years significantly more than 50 new bispidine based ligands were prepared and their coordination chemistry studied. Biological probes and medicinal applications is one main area in bispidine coordination chemistry, where fast complex formation, high stability, metal ion selectivity and inertness are of utmost importance. Oxygen activation and oxidation catalysis is another main focus in bispidine coordination chemistry, with catalyst efficiency and stability as well as product selectivity as important requirements. Particularly successful applications in these areas are presented and discussed in detail, in addition to fundamental principles that show the importance of ligand rigidity, cavity size and shape as overarching fundamental properties.

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比斯必定配位化学
铋是一种极刚性的配体,易于制备,品种繁多,具有4到10个齿,各种给体集和电荷,适用于单核和寡核过渡金属,主基团和稀土配合物。在最后的大约。20年来制备了50多种新型比斯必啶配体,并对其配位化学进行了研究。生物探针和医学应用是比斯必定配位化学的一个主要领域,其快速络合物形成、高稳定性、金属离子选择性和惰性是其重要的研究方向。氧活化和氧化催化是比斯必定配位化学的另一个主要研究方向,催化剂的效率和稳定性以及产物的选择性是重要的要求。特别成功的应用,在这些领域提出并详细讨论,除了基本原则,显示配体刚度,腔的大小和形状的重要性,作为首要的基本性质。
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来源期刊
Dalton Transactions
Dalton Transactions 化学-无机化学与核化学
CiteScore
6.60
自引率
7.50%
发文量
1832
审稿时长
1.5 months
期刊介绍: Dalton Transactions is a journal for all areas of inorganic chemistry, which encompasses the organometallic, bioinorganic and materials chemistry of the elements, with applications including synthesis, catalysis, energy conversion/storage, electrical devices and medicine. Dalton Transactions welcomes high-quality, original submissions in all of these areas and more, where the advancement of knowledge in inorganic chemistry is significant.
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