Solid polymorphism and dynamic magnetic properties of a dodecylated vanadyl–porphyrinato complex: spin–lattice relaxations modulated by phase stabilisation-Reference-Cited by-同舟云学术

Solid polymorphism and dynamic magnetic properties of a dodecylated vanadyl–porphyrinato complex: spin–lattice relaxations modulated by phase stabilisation

Published:2022 Issue:23 Volume:9 Page:6271-6278
ISSN:2052-1553
Container-title:Inorganic Chemistry Frontiers
language:en
Short-container-title:Inorg. Chem. Front.

Author:

Horii Yoji¹^ORCID,Makino Momo¹,Yamamoto Taro²,Tatsumi Shoichi²,Suzuki Hal²^ORCID,Noguchi Mariko³^ORCID,Yoshida Takefumi⁴,Kajiwara Takashi¹^ORCID,Li Zhao-Yang⁵^ORCID,Yamashita Masahiro⁵⁶^ORCID

Affiliation:

1. The Department of Chemistry, Faculty of Science, Nara Women's University, Nara 6308506, Japan

2. Department of Chemistry, Kindai University, 3-4-1 Kowakae, Higashiosaka, Osaka 577-8502, Japan

3. Graduate School of Integrated Basic Sciences, Nihon University, 3-25-40 Sakurajosui, Setagaya-ku, Tokyo 156-8550, Japan

4. Innovation Research Center for Fuel Cells, The University of Electro-Communications, Chofu, Tokyo 182-8585, Japan

5. School of Materials Science and Engineering, Nankai University, Tianjin 300350, China

6. Graduate School of Science, Tohoku University, 6-3 Aramaki-Aza-Aoba Aoba-ku, Sendai, Miyagi, 980-8578, Japan

Abstract

Phase stabilisation elongates spin–lattice relaxation times.

Funder

Higher Education Discipline Innovation Project

National Natural Science Foundation of China

Japan Society for the Promotion of Science

High Energy Accelerator Research Organization

Publisher

Royal Society of Chemistry (RSC)

Subject

Inorganic Chemistry

Link

http://pubs.rsc.org/en/content/articlepdf/2022/QI/D2QI01607A

Reference35 articles.

1. Electronic read-out of a single nuclear spin using a molecular spin transistor

2. Molecular spins for quantum computation

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4. Lanthanide Double-Decker Complexes Functioning as Magnets at the Single-Molecular Level

5. Quantum Coherence Times Enhancement in Vanadium(IV)-based Potential Molecular Qubits: the Key Role of the Vanadyl Moiety

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