1997
DOI: 10.1016/s1381-1169(97)00075-7
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Synthesis, structural characterization and catalytic carbonylation of nitrobenzene to phenylurethane using palladium (II) 1,10-phenanthroline diacetato complex

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Cited by 14 publications
(7 citation statements)
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“…Catalytic activity in the reaction was found for rhodium [1][2][3], ruthenium [4][5][6], palladium [7][8][9][10] and selenium [11][12][13] compounds. The palladium catalysts, on account of their relatively lower price and a high activity and selectivity, arouse greater interest.…”
Section: Introductionmentioning
confidence: 99%
See 1 more Smart Citation
“…Catalytic activity in the reaction was found for rhodium [1][2][3], ruthenium [4][5][6], palladium [7][8][9][10] and selenium [11][12][13] compounds. The palladium catalysts, on account of their relatively lower price and a high activity and selectivity, arouse greater interest.…”
Section: Introductionmentioning
confidence: 99%
“…However, this mechanism has not as yet been conclusively learnt. One of the suggested mechanisms is a direct carbonylation of nitrobenzene to carbamate by an intermediate nitrene stage [7,10]. Alternatively, Leconte et al [28] isolated a palladocyclic intermediate from the reaction of nitrobenzene with CO and proposed this as an intermediate.…”
Section: Introductionmentioning
confidence: 99%
“…However, this mechanism has not as yet been conclusively learnt. One of the suggested mechanisms is a direct carbonylation of nitrobenzene to carbamate by an intermediate nitrene stage [30]. Some authors agree that this reaction proceeds via an intermediate stage of aniline formation, which is subsequently directly carbonylated to carbamate [30,31].…”
Section: Hplc Analysis Of the Reduction Product Of Nbmentioning
confidence: 99%
“…One of the suggested mechanisms is a direct carbonylation of nitrobenzene to carbamate by an intermediate nitrene stage [30]. Some authors agree that this reaction proceeds via an intermediate stage of aniline formation, which is subsequently directly carbonylated to carbamate [30,31]. An alternative mechanism postulated involves aniline carbonylation to isocyanate, which immediately reacts with the excess aniline to afford diphenylurea [32,33].…”
Section: Hplc Analysis Of the Reduction Product Of Nbmentioning
confidence: 99%
“…The catalysts mostly used are salts or complexes of rhodium [4,5] ruthenium [6,7] and palladium [8][9][10] as well as selenium [11] and sulfur [12,13].…”
Section: Introductionmentioning
confidence: 99%