Unexpected trends in halogen-bond based noncovalent adducts

dc.contributor.author	Huber, Stefan M.
dc.contributor.author	Jiménez Izal, Elisa
dc.contributor.author	Ugalde Uribe-Etxebarria, Jesús
dc.contributor.author	Infante, Iván
dc.date.accessioned	2024-02-09T12:35:48Z
dc.date.available	2024-02-09T12:35:48Z
dc.date.issued	2012-06-14
dc.identifier.citation	Chemical Communications 48(62) : 7708-7710 (2012)	es_ES
dc.identifier.issn	1359-7345
dc.identifier.uri	http://hdl.handle.net/10810/65916
dc.description.abstract	Unexpected trends in the strengths of halogen-bond based adducts of CY3I (Y = F, Cl, Br, I) with two typical Lewis bases (chloride and trimethylamine) show that the halogen-bond donor strength (Lewis acidity) of a compound R–X is not necessarily increased with higher electronegativity of the (carbon-based) group R.	es_ES
dc.language.iso	eng	es_ES
dc.publisher	RSC	es_ES
dc.relation.isversionof	https://pubs.rsc.org/en/content/articlelanding/2012/cc/c2cc33304j
dc.rights	info:eu-repo/semantics/openAccess	es_ES
dc.title	Unexpected trends in halogen-bond based noncovalent adducts	es_ES
dc.type	info:eu-repo/semantics/article	es_ES
dc.rights.holder	RSC	es_ES
dc.rights.holder	© The Royal Society of Chemistry 2012
dc.identifier.doi	10.1039/C2CC33304J
dc.departamentoes	Polímeros y Materiales Avanzados: Física, Química y Tecnología
dc.departamentoeu	Polimero eta Material Aurreratuak: Fisika, Kimika eta Teknologia
dc.identifier.eissn	1364-548X