Supramolecular control of the template-induced selective photodimerization of 4-methyl-7-O-hexylcoumarin

Chemistry. 2003 Nov 21;9(22):5560-6. doi: 10.1002/chem.200305268.

Abstract

A symmetric ditopic molecular receptor (3), containing two identical hydrogen-bonding recognition subunits, was designed and synthesized. These subunits are capable of binding substrates with complementary donor and acceptor sites to form a supramolecular complex through hydrogen bonding. Receptor 3 was designed to accept two guest molecules, which are held in close proximity within the supramolecular species. The substrate molecule, 4-methyl-7-O-hexylcoumarin (1 c), forms a 2:1 complex with a binding constant of 150 m(-1) for the second substrate, passing first through a 1:1 complex with an affinity constant of 510 m(-1). The orientation of two molecules of 1 c when bound to the template leads to the selective formation of the trans-syn [2+2] photoproduct 2 cB upon irradiation. Other photoproducts typically produced in the absence of the template are suppressed.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Coumarins / chemistry*
  • Dimerization
  • Hydrogen Bonding
  • Photochemistry

Substances

  • Coumarins