Volume-conserving mechanism Hula twist

The hula twist mechanism (HT, Fig. 2.3B), first validated with carotenoids, is not consistent with the time-scale of photoisomerization of chromoproteins since CTI of the retinal chromophore, which is inserted deep inside the protein, necessitates a major reorganization of the peptide molecular framework. Therefore, a new volume-conserving mechanism, called bicyclic pedal (BP, Fig. 2.3C), was proposed. In fact, all these mechanisms are still a topic of discussion since chromoprotein photo-intermediates highlighted by recent studies do not confirm this hypothesis. In particular, several photo-products of the retinal Schiff base in the... 

A volume-conserving mechanism such as hula-twist (H-T) that requires a concomitant twisting of the double bond and the adjacent single bond to accomphsh the double-bond ds-trans isomerization, different from the usual one-bond rotation mechanism. 

The photoisomerization of all-s-trans-all-trans 1,3,5,7-octatetraene at 4.3 K illustrates the need for a new mechanism to explain the observed behavior [150]. Upon irradiation, all-s-trans-all-trans 1,3,5,7-octatetraene at 4.3 K undergoes conformational change from all-s-trans to 2-s-cis. Based on NEER principle (NonEquilibrium of Excited state Rotamers), that holds good in solution, the above transformation is not expected. NEER postulate and one bond flip mechanism allow only trans to cis conversion rotations of single bonds are prevented as the bond order between the original C C bonds increases in the excited state. However, the above simple photochemical reaction is explainable based on a hula-twist process. The free volume available for the all-s-trans-all-trans 1,3,5,7-octatetraene in the //-octane matrix at 4.3 K is very small and under such conditions, the only volume conserving process that this molecule can undergo is hula-twist at carbon-2. 

Three different photoisomerization mechanisms of singlet excited polyenes have been proposed (1) one-bond twist, a typical process observed in fluid solutions but also in glassy media,525 553 565 (2) the bicycle-pedal mechanism involving simultaneous rotation about two original double bonds, assumed to occur in a constraining environment,566-568 and (3) a volume-conserving two-bond hula twist 531 569 510 (Scheme 6.7). In some cases, the existence of the last mechanism has been ruled... 

If the assignments in Scheme 7 are correct, formation of the Tachy products involves rotations at adjacent double and single bonds, providing the first experimental verification of an outcome consistent with Liu s hula-twist mechanism for ds— trans photoisomerization. They have stimulated the recent resurrection of this mechanism with spedal attention to the key role of the volume-conserving requirements of the rigid medium. ... 

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