|1.||Niklasson, Anders M N: 1 article (02/2015)|
|2.||Cawkwell, M J: 1 article (02/2015)|
|3.||Dattelbaum, Dana M: 1 article (02/2015)|
|4.||Tschan, Mathieu J-L: 1 article (01/2007)|
|5.||Therrien, Bruno: 1 article (01/2007)|
|6.||Chérioux, Frédéric: 1 article (01/2007)|
|7.||Süss-Fink, Georg: 1 article (01/2007)|
|8.||Brezinsky, K: 1 article (08/2006)|
|9.||Sivaramakrishnan, R: 1 article (08/2006)|
|10.||Tranter, Robert S: 1 article (08/2006)|
02/14/2015 - "The initial chemical events that occur during the shock compression of liquid phenylacetylene have been investigated using self-consistent tight binding molecular dynamics simulations. "
02/14/2015 - "Extended Lagrangian Born-Oppenheimer molecular dynamics simulations of the shock-induced chemistry of phenylacetylene."
02/14/2015 - "Our simulations revealed that the first density-increasing step under shock compression arises from the polymerization of phenylacetylene molecules at the acetylene moiety. "
08/03/2006 - "A variety of stable species, ranging from small hydrocarbons to single ring aromatics (principal soot precursors such as phenylacetylene and indene) were sampled from the shock tube and analyzed using standard gas chromatographic techniques. "
01/01/2007 - "The hypothesis of molecular catalysis by dinuclear ruthenium complexes is supported by catalyst-poisoning experiments, the absence of an induction period in the kinetics of cyclohexene hydrogenation, and the isolation and single-crystal X-ray structure analysis of the tetrafluoroborate salt of the cation [(C(6)Me(6))(2)Ru(2)(PPh(2))(CHCHPh)H](+) (2), which can be considered as an intermediate in the case of phenylacetylene hydrogenation. "