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Farrell, David; Harding, Charles J.; McKee, Vickie and Nelson, Jane
(2006).
DOI: https://doi.org/10.1039/b602003h
Abstract
Treatment of N-methyl substituted aminocryptand hosts with copper(II) generates monocopper(II)
cryptates where copper(II) coordinates an oxygen-centered species, formally H3O+, which is also
strongly hydrogen bonded to three aminocryptand N-methyl atoms via bonds which may best be
viewed as NHd+ · · ·Od− in consequence of charge transfer. The strength of this hydrogen bonding
precludes successful competition of another copper ion for the second coordination site thus
suppressing formation of any Cu–Cu bonded average-valent system.
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About
- Item ORO ID
- 5220
- Item Type
- Journal Item
- ISSN
- 1477-9226
- Extra Information
- Some of the symbols may not have transferred correctly into this bibliographic record.
- Academic Unit or School
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Faculty of Science, Technology, Engineering and Mathematics (STEM) > Life, Health and Chemical Sciences
Faculty of Science, Technology, Engineering and Mathematics (STEM) - Depositing User
- Charlie Harding