1987
DOI: 10.1016/0009-2614(87)85028-5
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The production of Te atoms by the multiphoton dissociation of diethyltelluride

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Cited by 10 publications
(3 citation statements)
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“…As shown previously, 11 the observed dominance of ethene over n-butane and ethane is not in keeping with the previously assumed 20 homolysis of the C-M bonds. In accordance with the known disproportionation (2C 2 H 5 Á → C 2 H 4 C 2 H 6 )/combination (2C 2 H 5 Á → n-C 4 H 10 ) rate ratio k d /k c for the ethyl radical ($0.13), 21 a clean M-C homolysis would have yielded n-butane in a large excess over equal amounts of ethane and ethene.…”
Section: Photolysis Mechanismcontrasting
confidence: 37%
See 1 more Smart Citation
“…As shown previously, 11 the observed dominance of ethene over n-butane and ethane is not in keeping with the previously assumed 20 homolysis of the C-M bonds. In accordance with the known disproportionation (2C 2 H 5 Á → C 2 H 4 C 2 H 6 )/combination (2C 2 H 5 Á → n-C 4 H 10 ) rate ratio k d /k c for the ethyl radical ($0.13), 21 a clean M-C homolysis would have yielded n-butane in a large excess over equal amounts of ethane and ethene.…”
Section: Photolysis Mechanismcontrasting
confidence: 37%
“…19 The ArF and KrF laser photolysis of diethyl tellurium was shown to be a one-photon process at pulse energies as low as 2-6 mJ. 8 This conclusion was also drawn for KrF laser photolysis of diethyl tellurium in the absence and excess of hydro- gen. [6][7][8]20 The linear dependence of the initial depletion rate of diethyl tellurium on the laser fluence (Fig. 1a) shows (see also Ref 11.…”
Section: Photolysis Of Diethyl Telluriummentioning
confidence: 99%
“…It was revealed that neutral Te atoms are mostly produced in the ground and the lowest excited states. The preferred dissociation path in the 358-395 nm excitation region was considered [ 44 ] to be formation of neutral fragments ( Scheme 2 , path a). Under similar excitation conditions in the 510-400 nm region, ethyl ions and neutral Te atoms were found as the main products [ 45 ] and the proposed mechanism involves dissociation of a C 2 H 5 -Te + or (C 2 H 5 ) 2 Te + intermediate and fragments ( Scheme 2 , path b).…”
Section: Deposition Of Chalcogenmentioning
confidence: 99%