Large molecular motions are tolerated in crystals of diamine double salt of trans-chlorocinnamic acids with trans-1,2-diaminocyclohexane
Data(s) |
12/05/2005
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Resumo |
Contrary to the general assumption that photoreactions in crystals may not proceed with large molecular motions, a pedal-like motion prompted by electronic excitation is believed to be involved during the β-dimer formation from the crystals of the diamine double salt of trans-2,4-dichlorocinnamic acid and trans-1,2-diaminocyclohexane. |
Formato |
application/pdf |
Identificador |
http://eprints.iisc.ernet.in/27567/2/large.pdf Natarajan, Arunkumar and Mague, Joel T and Venkatesan, K and Ramamurthy, V (2005) Large molecular motions are tolerated in crystals of diamine double salt of trans-chlorocinnamic acids with trans-1,2-diaminocyclohexane. In: Organic Letters, 7 (10). pp. 1895-1898. |
Publicador |
American Chemical Society |
Relação |
http://pubs.acs.org/doi/abs/10.1021/ol050330u http://eprints.iisc.ernet.in/27567/ |
Palavras-Chave | #Organic Chemistry |
Tipo |
Journal Article PeerReviewed |