Paving the way for the synthesis of a series of divalent actinide complexes: a theoretical perspective-Reference-Cited by-同舟云学术

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Paving the way for the synthesis of a series of divalent actinide complexes: a theoretical perspective

Published:2016 Issue:7 Volume:45 Page:3102-3110
ISSN:1477-9226
Container-title:Dalton Transactions
language:en
Short-container-title:Dalton Trans.

Author:

Wu Q.-Y.¹²³⁴⁵,Lan J.-H.¹²³⁴⁵,Wang C.-Z.¹²³⁴⁵,Cheng Z.-P.¹²³⁴⁵,Chai Z.-F.¹²³⁴⁵,Gibson J. K.⁶⁷⁸⁹,Shi W.-Q.¹²³⁴⁵

Affiliation:

1. Laboratory of Nuclear Energy Chemistry and Key Laboratory for Biomedical Effects of Nanomaterials and Nanosafety

2. Institute of High Energy Physics

3. Chinese Academy of Sciences

4. Beijing

5. China

6. Chemical Sciences Division

7. Lawrence Berkeley National Laboratory

8. Berkeley

9. USA

Abstract

A series of divalent actinide species were systematically studied to identify the interactions between the +2 actinide ions and Cp′ ligands.

Funder

National Natural Science Foundation of China

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2016/DT/C5DT04540A

Reference55 articles.

1. Synthesis of a Crystalline Molecular Complex of Y2+, [(18-crown-6)K][(C5H4SiMe3)3Y]

2. Identification of the +2 Oxidation State for Uranium in a Crystalline Molecular Complex, [K(2.2.2-Cryptand)][(C5H4SiMe3)3U]

3. Synthesis and Characterization of a Uranium(II) Monoarene Complex Supported by δ Backbonding

4. All the Lanthanides Do It and Even Uranium Does Oxidation State +2

5. Synthesis, structure, and reactivity of crystalline molecular complexes of the {[C5H3(SiMe3)2]3Th}1− anion containing thorium in the formal +2 oxidation state

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