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Assembly of high nuclearity clusters from a family of tripodal tris-carboxylate ligands

Argent, Stephen P.; Tarassova, Irina; Greenaway, Alex; Nowell, Harriot; Barnett, Sarah A.; Warren, Mark R.; Tang, Chiu C.; Morris, Christopher G.; Lewis, William; Champness, Neil R.; Schr�der, Martin; Blake, Alexander J.

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Authors

Irina Tarassova

Alex Greenaway

Harriot Nowell

Sarah A. Barnett

Mark R. Warren

Chiu C. Tang

Christopher G. Morris

William Lewis

Neil R. Champness

Martin Schr�der

Alexander J. Blake



Abstract

A family of four tris-carboxylic acid ligands 1,3,5-tris(4′-carboxybiphenyl-2-yl)benzene (H3L1), 1,3,5-tris-2-carboxyphenylbenzene (H3L2), 1,3,5-tris(4″-carboxy-para-terphenyl-2-yl)benzene (H3L3) and 1,3,5-tris(3′-carboxybiphenyl-2-yl)benzene (H3L4) have been synthesised and reacted with first row transition metal cations to give nine complexes which have been structurally characterised by X-ray crystallography. The ligands share a common design motif having three arms connected to a benzene core via three ortho-disubstituted phenyl linkers. The ligands vary in length and direction of the carboxylic acid functionalised arms and are all able to adopt tripodal conformations in which the three arms are directed facially. The structures of [Zn8(μ4-O)(L1)4(HCO2)2(H2O)0.33(DMF)2] (1a-Zn), [Co14(L2)6((μ3-OH)8(HCO2)2(DMF)4(H2O)6] (2-Co), [Ni14(L2)6(μ3-OH)8(HCO2)2(DMF)4(H2O)6] (2-Ni), [Zn8(μ4-O)(L3)4(DMF)(H2O)4(NO3)2] (3-Zn), [Ni5(μ-OH)4(L2)2(H2O)6(DMF)4] (5-Ni), [Co8(μ4-O)4(L4)4(DMF)3(H2O)] (6-Co) and Fe3(μ3-O)(L4)2(H2O)(DMF)2)] (7-Fe) contain polynuclear clusters surrounded by ligands (L1–4)3− in tripodal conformations. The structure of [Zn2(HL1)2(DMF)4] (1b-Zn) shows it to be a binuclear complex in which the two ligands (HL2)2− are partially deprotonated whilst {[Zn3(L2)2(DMF)(H2O)(C5H5N)]·6(DMF)}n (4-Zn) is a 2D coordination network containing {Zn2(RCO2)4(solv)2} paddlewheel units. The conformations of the ligand arms in the complexes have been analysed, confirming that the shared ortho-disubstituted phenyl ring motif is a powerful and versatile tool for designing ligands able to form high-nuclearity coordination clusters when reacted with transition metal cations.

Citation

Argent, S. P., Tarassova, I., Greenaway, A., Nowell, H., Barnett, S. A., Warren, M. R., …Blake, A. J. (2016). Assembly of high nuclearity clusters from a family of tripodal tris-carboxylate ligands. Polyhedron, 120, 18-29. https://doi.org/10.1016/j.poly.2016.04.029

Journal Article Type Article
Acceptance Date Apr 18, 2016
Online Publication Date Apr 30, 2016
Publication Date Dec 14, 2016
Deposit Date Sep 27, 2017
Publicly Available Date Sep 27, 2017
Journal Polyhedron
Print ISSN 0277-5387
Electronic ISSN 1873-3719
Publisher Elsevier
Peer Reviewed Peer Reviewed
Volume 120
Pages 18-29
DOI https://doi.org/10.1016/j.poly.2016.04.029
Keywords High nuclearity cluster; Metal-directed assembly; Carboxylate bridging; Basic carboxylate; Crystal structure
Public URL https://nottingham-repository.worktribe.com/output/833425
Publisher URL http://www.sciencedirect.com/science/article/pii/S0277538716301127
Additional Information This article is maintained by: Elsevier; Article Title: Assembly of high nuclearity clusters from a family of tripodal tris-carboxylate ligands; Journal Title: Polyhedron; CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.poly.2016.04.029; Content Type: article; Copyright: © 2016 Elsevier Ltd. All rights reserved.
Contract Date Sep 27, 2017

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