A versatile hard–soft N/S-ligand for metal coordination and cluster formation

Please use this identifier to cite or link to this item: http://hdl.handle.net/123456789/2547

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DC Field	Value	Language
dc.contributor.author	Singh, Sanjay	-
dc.date.accessioned	2020-12-03T05:47:55Z	-
dc.date.available	2020-12-03T05:47:55Z	-
dc.date.issued	2016	-
dc.identifier.citation	Chemical Communications, 52(62), pp. 9683-9686	en_US
dc.identifier.other	https://doi.org/10.1039/C6CC04805F	-
dc.identifier.uri	https://pubs.rsc.org/en/content/articlelanding/2016/cc/c6cc04805f#!divAbstract	-
dc.identifier.uri	http://hdl.handle.net/123456789/2547	-
dc.description	Only IISERM authors are available in the record.	-
dc.description.abstract	Deprotonation of the thialdiphosphazane [SPH(μ-NtBu)]2 with a range of metal-bases gives the stable dianion [S-P(μ-NtBu)]22-, which is valence-isoelectronic with the widely-used [RN-P(μ-NR)]22- ligand. Structural studies show that the new ligand has adaptable hard-soft character with respect to the coordinated metal centre and that its multidentate nature can be exploited to construct large cage architectures.	en_US
dc.language.iso	en	en_US
dc.publisher	Royal Society of Chemistry	en_US
dc.subject	Deprotonation	en_US
dc.subject	Cluster formation	en_US
dc.subject	Supramolecular chemistry	en_US
dc.subject	Precursor	en_US
dc.title	A versatile hard–soft N/S-ligand for metal coordination and cluster formation	en_US
dc.type	Article	en_US
Appears in Collections:	Research Articles

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