Poly(p-phenylenevinylene) Derivatives with Defined Conjugation Segments and Post-Polymerization Modification with Sterically Enshrouded Chromophores.

Two poly(p-phenylenevinylene) derivative alternating copolymers (P1-I and P2-I) have been prepared featuring iodo substituents and m-phenylene units to periodically disrupt conjugation. P1-I was derivatized with various chromophores to yield P1a-f. In P1a-f, the chromophores were positioned within a sterically protected pocket shielding them from interchain interactions so that intrachain interactions between polymer segments could be observed.

Steric coordination control of interchain interactions in conducting metallopolymers.

The solution processability of a conducting metallopolymer (CMP1) based on a 2,2'-bipyridyl (bipy) derivatized poly(p-phenylene vinylene) (PPV) backbone has been accomplished by the strategic placement of sterically demanding mesityl side chains. The enhanced solubility of CMP1 can be traced to the prevention of coordinative crosslinking between polymer chains. The sterically enforced 1:1 bipy/metal ratio was confirmed by job analysis of absorption spectroscopic titration data.

"Turn-on" fluorescent sensor for the selective detection of zinc ion by a sterically-encumbered bipyridyl-based receptor.

A sterically-encumbered 5,5'-distyryl-2,2'-bipyridyl derivative that enforces a 1:1 metal-to-ligand ratio acts as a selective turn-on sensor for Zn(2+) in THF.