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通过反应诱导的预组织策略组装异双核锕系金属-有机骨架。

Assembling a Heterobimetallic Actinide Metal-Organic Framework by a Reaction-Induced Preorganization Strategy.

机构信息

State Key Laboratory of Radiation Medicine and Protection, School for Radiological and Interdisciplinary Sciences (RAD-X) and Collaborative Innovation Center of Radiation Medicine of Jiangsu Higher Education Institutions, Soochow University, Suzhou, 215123, China.

出版信息

Angew Chem Int Ed Engl. 2023 Jul 17;62(29):e202306360. doi: 10.1002/anie.202306360. Epub 2023 Jun 12.

Abstract

Periodically arranging coordination-distinct actinides into one crystalline architecture is intriguing but of great synthetic challenge. We report a rare example of a heterobimetallic actinide metal-organic framework (An-MOF) by a unique reaction-induced preorganization strategy. A thorium MOF (SCU-16) with the largest unit cell among all Th-MOFs was prepared as the precursor, then the uranyl was precisely embedded into the MOF precursor under oxidation condition. Single crystal of the resulting thorium-uranium MOF (SCU-16-U) shows that a uranyl-specific site was in situ induced by the formate-to-carbonate oxidation reaction. The heterobimetallic SCU-16-U exhibits multifunction catalysis properties derived from two distinct actinides. The strategy proposed here offers a new avenue to create mixed-actinide functional material with unique architecture and versatile functionality.

摘要

周期性地将配位不同的锕系元素排列成一个晶体结构是很吸引人的,但具有很大的合成挑战性。我们通过独特的反应诱导预组织策略报告了一个罕见的异金属锕系元素金属有机骨架(An-MOF)的例子。一个钍 MOF(SCU-16)具有所有 Th-MOF 中最大的晶胞,被制备为前体,然后在氧化条件下将铀酰精确嵌入 MOF 前体中。所得到的钍-铀 MOF(SCU-16-U)的单晶表明,一个铀酰特定的位置是由甲酸盐到碳酸盐的氧化反应原位诱导的。异双金属 SCU-16-U 表现出源自两种不同锕系元素的多功能催化性质。这里提出的策略为创造具有独特结构和多功能的混合锕系元素功能材料提供了一条新途径。

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