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The thermal cis-trans isomerization of azobenzene, stilbene, N-benzylideneaniline and some of their derivatives in the vapour phase at elevated temperatures studied by flash photolysisAndersson, Jan-Åke. January 1983 (has links)
Thesis--Uppsala. / In Periodical Room.
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Parawasserstoffumwandlung an seltenen Erd-Oxiden Untersuchung des magnetokatalytischen Effekts /Jugel, Joachim, January 1980 (has links)
Thesis (doctoral)--München, 1980.
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Experimental observation and quantum chemical investigation of thallium(I) (Z)-methanediazotate: synthesis of a long sought and highly reactive speciesSingh, Neeraj, Fiedler, Benjamin, Friedrich, Joachim, Banert, Klaus 28 April 2017 (has links) (PDF)
For the first time, successful synthesis and characterisation of the missing (Z)-isomer of thallium(I) methanediazotate has been accomplished, utilising low-temperature NMR monitoring analysis. The title compound was synthesised from N-methyl-N-nitrosourea and thallium(I) propoxide, under sub-ambient temperature conditions, as a highly moisture sensitive entity. Quantum chemical calculations, performed at the CCSD(T) level, depict excellent conformity to experimental results. Indeed, compared to its (E) counterpart, the formation of the title compound is thermodynamically less favoured, but preferred by means of kinetic control owing to a hindered isomerisation.
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Experimental observation and quantum chemical investigation of thallium(I) (Z)-methanediazotate: synthesis of a long sought and highly reactive speciesSingh, Neeraj, Fiedler, Benjamin, Friedrich, Joachim, Banert, Klaus 28 April 2017 (has links)
For the first time, successful synthesis and characterisation of the missing (Z)-isomer of thallium(I) methanediazotate has been accomplished, utilising low-temperature NMR monitoring analysis. The title compound was synthesised from N-methyl-N-nitrosourea and thallium(I) propoxide, under sub-ambient temperature conditions, as a highly moisture sensitive entity. Quantum chemical calculations, performed at the CCSD(T) level, depict excellent conformity to experimental results. Indeed, compared to its (E) counterpart, the formation of the title compound is thermodynamically less favoured, but preferred by means of kinetic control owing to a hindered isomerisation.
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