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金属-金属到配体电荷转移激发态和发光钳钯-异氰化物配合物的超分子聚合。

The Metal-Metal-to-Ligand Charge Transfer Excited State and Supramolecular Polymerization of Luminescent Pincer Pd -Isocyanide Complexes.

机构信息

State Key Laboratory of Synthetic Chemistry, Institute of Molecular Functional Materials, Department of Chemistry, The University of Hong Kong, Pokfulam Road, Hong Kong SAR, China.

HKU Shenzhen Institute of Research and Innovation, Shenzhen, Guangdong, 518053, China.

出版信息

Angew Chem Int Ed Engl. 2018 Mar 12;57(12):3089-3093. doi: 10.1002/anie.201712249. Epub 2018 Feb 2.

Abstract

Pincer Pd -isocyanide complexes are described that display intermolecular interactions and emissive MMLCT excited states in aggregation state(s) at room temperature. The intermolecular Pd -Pd and ligand-ligand interactions drive these complexes to undergo supramolecular polymerization in a living manner. Comprehensive spectroscopic studies reveal a pathway with a kinetic trap that can be modulated by changing the counteranion and metal atom. The Pd supramolecular assemblies comprise two different aggregation forms with only one to be emissive. DFT/TDDFT calculations lend support to the MMLCT absorption and emission of these pincer Pd -isocyanide aggregates.

摘要

夹式 Pd-异氰化物配合物具有分子间相互作用和室温下聚集态的发射 MMLCT 激发态。分子间 Pd-Pd 和配体-配体相互作用促使这些配合物以活性质点的方式进行超分子聚合。全面的光谱研究揭示了一种具有动力学陷阱的途径,通过改变抗衡阴离子和金属原子可以对其进行调节。Pd 超分子组装由两种不同的聚集形式组成,只有一种是发光的。DFT/TDDFT 计算支持这些夹式 Pd-异氰化物聚集体的 MMLCT 吸收和发射。

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