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dc.date.accessioned 2019-10-04T15:59:52Z
dc.date.available 2019-10-04T15:59:52Z
dc.date.issued 2009
dc.identifier.uri http://sedici.unlp.edu.ar/handle/10915/82738
dc.description.abstract The crystal structures of heptamethylenediammonium bis(saccharinate) monohydrate, [H3N-(CH2)7-NH3J(sac) 2-H2O(1) and octamethylenediammonium bis(saccharinate) hemihydrate, [H3N-(CH2)8-NH3J(sac) 2-0.5H2O(2), were determined by single-crystal X-ray diffraction methods. Compound 1 crystallizes in the triclinic space group PI with 2 molecules per unit cell, and 2 in the mono-clinic space group P2 1/a with Z = 4. The saccharinate moiety is planar in both compounds presenting bonding characteristics comparable to those found in other saccharinate salts. The ionic crystals are fürther stabilized by an extensive H-bonding network, which links the anions and cations into an infinite three-dimensional supramolecular assembly. The FTIR spectra of the adducts are briefly discussed in comparison with those of the constituent molecules. en
dc.format.extent 1041-1045 es
dc.language en es
dc.subject Crystal Structures es
dc.subject Heptamethylenediammonium bis(saccharinate) Monohydrate es
dc.subject IR Spectra es
dc.subject Octamethylenediammo- nium Bis(saccharinate) Hemihydrate es
dc.subject Supramolecular Adducts es
dc.title Two new supramolecular assemblies obtained by reaction between saccharin and long-chain diamines en
dc.type Articulo es
sedici.identifier.other doi:10.1515/znb-2009-0908 es
sedici.identifier.other eid:2-s2.0-70349303739 es
sedici.identifier.issn 0932-0776 es
sedici.creator.person Castellano, Eduardo Ernesto es
sedici.creator.person Piro, Oscar Enrique es
sedici.creator.person Parajón Costa, Beatriz S. es
sedici.creator.person Barán, Enrique José es
sedici.subject.materias Química es
sedici.description.fulltext true es
mods.originInfo.place Facultad de Ciencias Exactas es
mods.originInfo.place Centro de Química Inorgánica es
sedici.subtype Articulo es
sedici.rights.license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)
sedici.rights.uri http://creativecommons.org/licenses/by-nc-sa/4.0/
sedici.description.peerReview peer-review es
sedici.relation.journalTitle Zeitschrift fur Naturforschung - Section B Journal of Chemical Sciences es
sedici.relation.journalVolumeAndIssue vol. 64, no. 9 es


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Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0) Excepto donde se diga explícitamente, este item se publica bajo la siguiente licencia Creative Commons Attribution-NonCommercial-ShareAlike 4.0 International (CC BY-NC-SA 4.0)