Catalysts function by providing an alternate reaction mechanism that has a lower activation energy than would be found in the absence of the catalyst. In some cases, the catalyzed mechanism may include additional steps. 31608-22-7, Name is 2-(4-Bromobutoxy)tetrahydro-2H-pyran, molecular formula is C9H17BrO2. In a Article，once mentioned of 31608-22-7, Recommanded Product: 31608-22-7
The rhenium(I) and ruthenium(II) complexes of a fullerene-substituted bipyridine ligand have been prepared. Electrochemical studies indicate that some ground state electronic interaction between the fullerene subunit and the metal-complexed moiety are present in the ReI but not the RuII complex. The photophysical properties have been investigated by steady-state and time-resolved UV/Vis-NIR luminescence spectroscopy and nanosecond laser flash photolysis in CH2Cl2 solution, and compared to those of the corresponding model compounds. Excitation of the methanofullerene moiety in the dyads does not lead to excited state intercomponent interactions. Instead, excitation of the metal-complexed unit shows that the lowest triplet metal-to-ligand-charge-transfer excited state (3MLCT) centered on the ReI- or RuIItype unit is quenched with a rate constant of about 2.5 × 108 s-1. The quenching is attributed to an electron-transfer (E1T) process leading to the reduction of the carbon sphere, as determined by luminescence spectroscopy for the RuII dyad. Experimental detection of electron transfer in the ReI dyad is prevented due to the unfavorable absorption of the metal-complexed moiety relative to the fullerene unit. However, it can be postulated on the basis of energetic/kinetic arguments and by comparison with the RuII-type array. The primary E1T process is followed by charge-recombination to give the lowest-lying fullerene triplet excited state (3C60) with quantitative yield, as determined by sensitized singlet oxygen luminescence experiments. Direct 3MLCT ? 3C60 triplet-triplet energy-transfer (EnT) does not successfully compete with E1T since it is highly exoergonic and located in the Marcus inverted region. The quantum yield of singlet oxygen sensitization (phiDelta) of the RuI-based dyad is found to be lower (0.80) than for the corresponding RuII derivative (1.0). This is likely to be the consequence of different conformational structures for the two dyads, rather than a different yield of 3C60 formation.
Note that a catalyst decreases the activation energy for both the forward and the reverse reactions and hence accelerates both the forward and the reverse reactions.Recommanded Product: 31608-22-7, you can also check out more blogs about31608-22-7
Reference：
Tetrahydropyran – Wikipedia,
Tetrahydropyran – an overview | ScienceDirect Topics