Investigating the conformations of a family of [M2L3]4+ helicates using single crystal X-ray diffraction

Matthew J. Wallis; Hyunsung Min; Leonard F. Lindoy; Feng Li

Investigating the conformations of a family of [M2L3]4+ helicates using single crystal X-ray diffraction

Matthew J. Wallis, Hyunsung Min, Leonard F. Lindoy, Feng Li

Western Sydney University

Research output: Contribution to journal › Article › peer-review

6 Citations (Scopus)

Abstract

We present five new dinuclear triple helicate compounds of types [Mn2L3](ClO4)4, [Co2L3](BF4)4, [Ni2L3](BF4)4, [Cu2L3](BF4)4, and [Zn2L3](BF4)4, where L is a previously reported semi-rigid ligand incorporating two α-diimine primary donor groups and two secondary 4-pyridyl donor groups. All complexes have been characterized in both solution and the solid state. Single crystal X-ray diffraction studies were used to probe the variation in the respective helical structures as the coordinated metal ion was altered, including the effect on the orientations of the secondary binding domains. The influence of the metal ion size, the spin state in the case of Fe(II), and the presence of Jahn-Teller distortions on the overall helical structure has been investigated. These results form a basis for the design and construction of new large metallosupramolecular architectures which manifest properties associated with the constituent helical metalloligand units.

Original language	English
Article number	1404
Number of pages	12
Journal	Molecules
Volume	28
Issue number	3
Publication status	Published - Feb 2023

Open Access - Access Right Statement

© 2023 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).

Cite this

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title = "Investigating the conformations of a family of [M2L3]4+ helicates using single crystal X-ray diffraction",

abstract = "We present five new dinuclear triple helicate compounds of types [Mn2L3](ClO4)4, [Co2L3](BF4)4, [Ni2L3](BF4)4, [Cu2L3](BF4)4, and [Zn2L3](BF4)4, where L is a previously reported semi-rigid ligand incorporating two α-diimine primary donor groups and two secondary 4-pyridyl donor groups. All complexes have been characterized in both solution and the solid state. Single crystal X-ray diffraction studies were used to probe the variation in the respective helical structures as the coordinated metal ion was altered, including the effect on the orientations of the secondary binding domains. The influence of the metal ion size, the spin state in the case of Fe(II), and the presence of Jahn-Teller distortions on the overall helical structure has been investigated. These results form a basis for the design and construction of new large metallosupramolecular architectures which manifest properties associated with the constituent helical metalloligand units.",

author = "Wallis, {Matthew J.} and Hyunsung Min and Lindoy, {Leonard F.} and Feng Li",

year = "2023",

month = feb,

language = "English",

volume = "28",

journal = "Molecules",

issn = "1420-3049",

publisher = "MDPI AG",

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TY - JOUR

T1 - Investigating the conformations of a family of [M2L3]4+ helicates using single crystal X-ray diffraction

AU - Wallis, Matthew J.

AU - Min, Hyunsung

AU - Lindoy, Leonard F.

AU - Li, Feng

PY - 2023/2

Y1 - 2023/2

N2 - We present five new dinuclear triple helicate compounds of types [Mn2L3](ClO4)4, [Co2L3](BF4)4, [Ni2L3](BF4)4, [Cu2L3](BF4)4, and [Zn2L3](BF4)4, where L is a previously reported semi-rigid ligand incorporating two α-diimine primary donor groups and two secondary 4-pyridyl donor groups. All complexes have been characterized in both solution and the solid state. Single crystal X-ray diffraction studies were used to probe the variation in the respective helical structures as the coordinated metal ion was altered, including the effect on the orientations of the secondary binding domains. The influence of the metal ion size, the spin state in the case of Fe(II), and the presence of Jahn-Teller distortions on the overall helical structure has been investigated. These results form a basis for the design and construction of new large metallosupramolecular architectures which manifest properties associated with the constituent helical metalloligand units.

AB - We present five new dinuclear triple helicate compounds of types [Mn2L3](ClO4)4, [Co2L3](BF4)4, [Ni2L3](BF4)4, [Cu2L3](BF4)4, and [Zn2L3](BF4)4, where L is a previously reported semi-rigid ligand incorporating two α-diimine primary donor groups and two secondary 4-pyridyl donor groups. All complexes have been characterized in both solution and the solid state. Single crystal X-ray diffraction studies were used to probe the variation in the respective helical structures as the coordinated metal ion was altered, including the effect on the orientations of the secondary binding domains. The influence of the metal ion size, the spin state in the case of Fe(II), and the presence of Jahn-Teller distortions on the overall helical structure has been investigated. These results form a basis for the design and construction of new large metallosupramolecular architectures which manifest properties associated with the constituent helical metalloligand units.

UR - https://hdl.handle.net/1959.7/uws:69280

M3 - Article

SN - 1420-3049

VL - 28

JO - Molecules

JF - Molecules

IS - 3

M1 - 1404

ER -

Investigating the conformations of a family of [M2L3]4+ helicates using single crystal X-ray diffraction

Abstract

Open Access - Access Right Statement

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