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.
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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.
|Item Type:||Journal Article|
|Additional Information:||Copyright of this article belongs to American Chemical Society.|
|Department/Centre:||Division of Chemical Sciences > Organic Chemistry|
|Date Deposited:||04 Jun 2010 09:59|
|Last Modified:||19 Sep 2010 06:01|
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