126019-32-7Relevant academic research and scientific papers
Rotaxane or pseudorotaxane? Effects of small structural variations on the deslipping kinetics of rotaxanes with stopper groups of intermediate size
Affeld, Ansgar,Huehner, Gosia M.,Seel, Christian,Schalley, Christoph A.
, p. 2877 - 2890 (2007/10/03)
Three series of rotaxanes have been synthesized variously by slipping synthesis, in which axis and wheel are melted in admixture, by recognition of amide groups inside the macrocyclic wheel, or by an anionic template method, in which the stoppering phenol
Models for the charging of extended π chains
Schenk, Rainer,Gregorius, Heike,Meerholz, Klaus,Heinze, Jürgen,Mülen, Klaus
, p. 2634 - 2647 (2007/10/02)
The syntheses as well as the chemical and electrochemical reduction of a series of novel oligo(phenylenevinylenes) are described. The extended π chains are built up by sequences of Wittig reactions, and the corresponding polyanions are generated by electr
Cis-trans photoisomerization of a p-styrylstilbene, a one- and twofold adiabatic process
Sandros, Kjell,Sundahl, Mikael,Wennerstr?m, Olof,Norinder, Ulf
, p. 3082 - 3086 (2007/10/02)
The mechanism of the Z/E photoisomerization of a p-styrylstilbene has been studied by steady state and time-resolved fluorescence measurements combined with isomerization quantum yield determinations. It was found that on excitation of the Z,Z isomer both the isomers, Z,E and E,E, are produced initially, mainly by adiabatic processes on the singlet excited surface. Quantum mechanical calculations give surface profiles supporting the adopted mechanism.
Triplet State Z/E Isomerization of a p-Styrylstilbene, a Partly Adiabatic Process
Sundahl, Mikael,Wennerstroem, Olof,Sandros, Kjell,Arai, Tatsuo,Tokumaru, Katsumi
, p. 6731 - 6734 (2007/10/02)
The quantum yields for biacetyl-sensitized Z/E photoisomerization of the isomers of 3,3'',5,5''-tetra-tert-butyl-4'-styrylstilbene, ZZ, ZE, and EE, have been determined.ZZ and ZE showed increased isomerization quantum yields with increased concentration due to a quantum chain process with 3EE* as the chain-carrying species.The photostationary state consists of a mixture of ZE and EE with more of the latter at higher concentration.Addition of azulene to the photoisomerization reaction drastically increases the proportion of EE at the photostationary state from ca. 50percent to 99percent.The T1-Tn absorption spectra for all three isomers are identical as is the triplet lifetime (τ = 3.5 μs at 298 K).From a temperature study of the triplet lifetime (τ = 120 μs at 193 K) we conclude that there are two important triplet-state conformations: one with a planar E,E structure and the other where one double bond is twisted close to 90 deg.The energy difference between the two conformations was determined to be 4.4 +/- 0.5 kcal mol-1, with the planar structure being the more stable.From quenching experiments the triplet energy of EE was determined to be 41 kcal mol-1.
The Charge Storage Mechanism of Conducting Polymers: A Voltammetric Study on Defined Soluble Oligomers of the Phenylene-Vinylene Type
Heinze, Juergen,Mortensen, John,Muellen, Klaus,Schenk, Rainer
, p. 701 - 703 (2007/10/02)
The reductive charging-discharging behaviour of several newly synthesized soluble oligo-p-phenylene-vinylenes was studied by cyclic voltammetry; the results show that both the number of redox states and the magnitude of their energetic interaction depend
