Structural effects and hydrogen bonds on N,N `-di(methoxycarbonylsulfenyl)urea, [CH(3)OC(O)SNH](2)CO, studied by experimental and theoretical methods


Autoria(s): VALLEJOS, Sonia Torrico; ERBEN, Mauricio F.; BOESE, Roland; PIRO, Oscar E.; CASTELLANO, Eduardo Ernesto; VEDOVA, Carlos O. Della
Contribuinte(s)

UNIVERSIDADE DE SÃO PAULO

Data(s)

20/10/2012

20/10/2012

2009

Resumo

Pure N,N`-di(methoxycarbonylsulfenyl)urea, [CH(3)OC(O)SNH](2)CO, is quantitatively prepared by the hydrolysis reaction of CH(3)OC(O)SNCO and characterized by (1)H NMR, GC-MS and FTIR spectroscopy techniques. Structural and conformational properties are analyzed using a combined approach with data obtained from X-ray diffraction, vibrational spectra and theoretical calculation methods. The IR and Raman spectra for normal and deuterated species are reported. The crystal structure of [CH(3)OC(O)SNH](2)CO was determined by X-ray diffraction methods. The substance crystallizes in the orthorhombic P2(1)2(1)2 space group with a = 9.524(2), b = 12.003(1), c = 4.481 (1) angstrom, and Z = 2 moieties in the unit cell. The molecule is sited on a twofold crystallographic axis (C(2)) parallel to c and shows the anti-anti conformation (S-N single bonds antiperiplanar with respect to the opposite C-N single bonds in sulfenyl-urea-sic group). Neighboring molecules are arranged in a chain motif that extends along the C(2)-axis and is held by bifurcated NH center dot center dot center dot O center dot center dot center dot HN intermolecular bonds. A local planar symmetry is observed in the crystal for the central -SN(H)C(O)N(H)S- skeleton. Experimental and calculated data allow to trace this structural feature to the occurrence of N-H center dot center dot center dot O=C hydrogen bonding interactions. Calculated vibrational and structural properties are in good agreement with the experimentally determined features. (C) 2008 Elsevier B.V. All rights reserved.

Volkswagen-Stiftung

Volkswagen-Stiftung

Deutsche Forschungsgemeinschaft (DFG)

Deutsche Forschungsgemeinschaf (DFG)

ANPCYT-DAAD for the German-Argentinean cooperation Awards (PROALAR)

Deutscher Akademischer Austauschdienst (DAAD)

Agencia Nacional de Promoción Científica y Tecnológica (ANPCyT)

Deutscher Akademischer Austauschdienst (DAAD)

DAAD Regional Program of Chemistry for Argentina

Consejo Nacional de Investigaciones Científicas y Técnicas de Argentina (CONICET)

Consejo Nacional de Investigaciones Cientificas y Tecnicas (CONICET)

Comision de Investigaciones Cientificas de la Provincia de Buenos Aires (CIC), Republica Argentina

Comisión de Investigaciones Científicas Provincia de Buenos Aires (CIC) - Argentina

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

FAPESP, Brazil

Facultad de Ciencias Exactas, Universidad Nacional de La Plata

Facultad de Ciencias Exactas, Universidad Nacional de La Plata

Identificador

JOURNAL OF MOLECULAR STRUCTURE, v.918, n.1/Mar, p.146-153, 2009

0022-2860

http://producao.usp.br/handle/BDPI/29971

10.1016/j.molstruc.2008.07.031

http://dx.doi.org/10.1016/j.molstruc.2008.07.031

Idioma(s)

eng

Publicador

ELSEVIER SCIENCE BV

Relação

Journal of Molecular Structure

Direitos

restrictedAccess

Copyright ELSEVIER SCIENCE BV

Palavras-Chave #Hydrogen bonding #X-ray structure #Urea #Conformational study #CRYSTAL-FIELD METHODS #AB-INITIO #INTERMOLECULAR INTERACTIONS #VIBRATIONAL-SPECTRUM #NEUTRON-DIFFRACTION #AQUEOUS UREA #POLYSULFONYLAMINES #PSEUDOHALIDES #CONFORMATION #SPECTROSCOPY #Chemistry, Physical
Tipo

article

original article

publishedVersion