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Expanding and quantifying the crystal chemistry of the flexible ligand 15aneN5

Shircliff, Anthony D.; Davilla, Dustin J.; Allbritton, Elisabeth M. A.; Gorbet, Michael Joseph; Jones, Donald G.; Tresp, David S.; Allen, Michael B.; Shrestha, Alina; Burgess, Gwendolyn E.; Eze, John I.; Fernandez, Andrea T.; Ramirez, Daniel; Shoff, Kody J.; Crispin, Garet G.; Crone, Sarah B.; Flinn, Michael; Tran, Tien; Bryce, Darby S.; Bond, Abbagale L.; Shockey, Dylan W.; Oliver, Allen Grayson; Krause, Jeanette; Prior, Timothy J.; Hubin, Timothy J.

Authors

Anthony D. Shircliff

Dustin J. Davilla

Elisabeth M. A. Allbritton

Michael Joseph Gorbet

Donald G. Jones

David S. Tresp

Michael B. Allen

Alina Shrestha

Gwendolyn E. Burgess

John I. Eze

Andrea T. Fernandez

Daniel Ramirez

Kody J. Shoff

Garet G. Crispin

Sarah B. Crone

Michael Flinn

Tien Tran

Darby S. Bryce

Abbagale L. Bond

Dylan W. Shockey

Allen Grayson Oliver

Jeanette Krause

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Dr Tim Prior T.Prior@hull.ac.uk
Senior Lecturer in Inorganic Chemistry

Timothy J. Hubin



Abstract

Tetraazamacrocycles have been very extensively exploited as transition metal ligands for a variety of purposes, including catalysis, medical imaging, pharmaceuticals, etc. However, the pentaazamacrocycles are much less commonly used for similar purposes because of poor availability, difficulties in their synthesis, and less well-known metal coordination properties. 1,4,7,10,13-pentaazacyclopentadane (15aneN5) was initially synthesized by a published synthetic route, which we simplified and shortened with minimal drop in yield. Eight different transition metal complexes were made using typical complexation methods. X-ray crystallography of multiple novel complexes yielded insight into the flexibility in coordination geometry of this interesting macrocycle as well as the first crystal structures of 15aneN5 with Cr3+, Mn3+, Fe3+, Co3+, Cu2+, and Ru2+. A parameter to quantify the coordination geometry adopted by the ligand was devised and applied to all known crystal structures of its metal complexes. Finally, oxidation of 15aneN5 to a novel diimine macrocycle was observed during complexation with ruthenium.

Citation

Shircliff, A. D., Davilla, D. J., Allbritton, E. M. A., Gorbet, M. J., Jones, D. G., Tresp, D. S., …Hubin, T. J. (2022). Expanding and quantifying the crystal chemistry of the flexible ligand 15aneN5. CrystEngComm, 24(6), 1218-1236. https://doi.org/10.1039/d1ce01534f

Journal Article Type Article
Acceptance Date Jan 4, 2022
Online Publication Date Jan 13, 2022
Publication Date Feb 14, 2022
Deposit Date Jan 19, 2022
Publicly Available Date Jan 14, 2023
Journal CrystEngComm
Electronic ISSN 1466-8033
Publisher Royal Society of Chemistry
Peer Reviewed Peer Reviewed
Volume 24
Issue 6
Pages 1218-1236
DOI https://doi.org/10.1039/d1ce01534f
Keywords Condensed Matter Physics; General Materials Science; General Chemistry
Public URL https://hull-repository.worktribe.com/output/3913861

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©2022 The authors. All rights reserved. No part of this publication may be reproduced without the written permission of the copyright holder




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