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Isabelle Couturier-Tamburelli

Publications and source records attributed to Isabelle Couturier-Tamburelli.

4 recordsLinked to original sources

UV photolysis of C4N2 in water ices: new possible route of synthesis of ammonium bicarbonate and ammonium formate.

Laboratory experiments involving ultraviolet (UV) irradiation of dicyanoacetylene (C(4)N(2)) trapped in water ice at 10 K have been conducted and monitored by infrared spectroscopy (FTIR). By the support of isotopic experiments and theoretical calculations, the irradiation of a DCA/H(2)O ice mixture at lambda > 230 nm has been found to be a possible source of NH(4)(+)HCO(3)(-) (ammonium bicarbonate) and NH(4)(+)HCOO(-) (ammonium formate). These latter compounds can arise from a proton-transfer reaction between H(2)O and the CN radical, which is issued from photolyzed C(4)N(2).

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Photoreactivity of cyanoacetylene trapped in water ice: an infrared, isotopic and theoretical study.

Photoreactivity of cyanoacetylene with water was successively studied in cryogenic matrixes and in the solid phase at lambda > 120 nm. These studies were performed using FTIR spectroscopy, isotopic experiments and DFT calculations at the B3LYP/6-31G level of theory. The photolysis of cyanoacetylene complexed with water in an argon cryogenic matrix led to the formation of two products. The first one corresponds to the cyanoketene and the second to the HCN:C2O complex. Trapped in water ice and submitted to UV photolysis, the cyanoacetylene molecule shows great photoreactivity. Indeed, besides the cyanoketene and cyanhydric acid, we characterized and identified the formation of other compounds issued from the addition of water to the CC triple bond of cyanoacetylene.

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Breaking of ketene bonds during HCl addition to trimethylsilylketene.

IR spectroscopy is coupled with the matrix isolation technique to study the reaction of trimethylsilylketene with HCl. From 50 K trimethylsilylketene reacts with hydrogen chloride, leading to the cleavage of the Si-C bond and the formation of trimethylsilyl chloride and acetyl chloride, through intermediate trimethylsilylacetyl chloride which was identified. A reaction profile for this result is proposed based on a theoretical study carried out at the DFT level.

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Interstellar ice surface site modification induced by dicyanoacetylene adsorption.

Dicyanoacetylene adsorbed on amorphous ice water at 10 K presents an interaction with the dangling H site and induces a s(4) adsorption site formation due to the restructuring of the ice bulk. Warming up the sample provokes the dicyanoacetylene desorption from the H(2)O ice film, which could be due to the beginning of the ice crystallization process. The desorption activation energy measured by temperature-programmed desorption (E(d) = 42 +/- 5 kJ x mol(-1)) is in good agreement with that calculated (E(d) = 46 kJ x mol(-1)) and gives evidence of a hydrogen-bonded adsorbed state on amorphous ice films.

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