Radical Polymerization of Styrene Controlled by Half-Sandwich Mo(III)/Mo(IV) Couples: All Basic Mechanisms Are Possible

Overview & Synopsis

Density functional calculations of bond dissociation energies (BDEs) have been used as a guide to the choice of metal system suitable for controlling styrene polymerization by either the stable free radical polymerization (SFRP) or the atom transfer radical polymerization (ATRP) mechanism. In accord with the theoretical prediction, CpMo(η4-C4H6)(CH2SiMe3)2, 2, is not capable of yielding SFRP of styrene. Still in accord with theoretical prediction, CpMo(η4-C4H6)Cl2, 1, CpMo(PMe3)2Cl2, 3, and CpMo(dppe)Cl2 (dppe = 1,2-bis(diphenylphosphino)ethane), 4, yield controlled styrene polymerization by the SFRP mechanism in the presence of 2,2‘-azobisisobutyronitrile (AIBN). This arises from the generation of a putative Mo(IV) alkyl species from the AIBN-generated radical addition to the Mo(III) compound. The controlled nature of the polymerizations is indicated by linear Mn progression with the conversion in all cases and moderate polydispersity indices (PDIs). Controlled polymerization of styrene is also given by compounds 3 and 4 in combination with alkyl bromides. These complexes then operate by the ATRP mechanism, again in accord with the theoretical predictions. Controlled character is revealed by linear increase of Mn versus conversion, low PDIs, a stop-and-go experiment, and 1H NMR and MALDI-TOF analyses of the polymer end groups. The same controlled polymerization is given by a “reverse” ATRP experiment, starting from AIBN and CpMo(PMe3)2Cl2Br, 5. On the other hand, when compound 1 or 2 is used in combination with an alkyl bromide (as for an ATRP experiment), the isolated polystyrene shows by Mn, 1H NMR, and MALDI-TOF analyses that catalytic chain transfer (CCT) radical polymerization takes place in this case. Kinetics simulations underscore the conditions regulating the radical polymerization mechanism and the living character of the polymerization. The complexes herein described are ineffective at controlling the polymerization of methyl methacrylate.