Primary Radical Cations in Irradiated Poly(isobutylene)

Vsevolod I Borovkov; Pavel A Potashov; Irina V Beregovaya; Lyudmila N Shchegoleva; Yuri N Molin

doi:10.1021/acs.jpcb.0c03280

Primary Radical Cations in Irradiated Poly(isobutylene)

J Phys Chem B. 2020 Aug 13;124(32):7059-7066. doi: 10.1021/acs.jpcb.0c03280. Epub 2020 Aug 4.

Authors

Vsevolod I Borovkov^{1

2}, Pavel A Potashov^{1

2}, Irina V Beregovaya³, Lyudmila N Shchegoleva³, Yuri N Molin¹

Affiliations

¹ Voevodsky Institute of Chemical Kinetics and Combustion, SB RAS, 3, Institutskaya str., 630090 Novosibirsk, Russia.
² Novosibirsk State University, 2, Pirogova str., Novosibirsk 630090, Russia.
³ N. N. Vorozhtsov Novosibirsk Institute of Organic Chemistry, SB RAS, 9, Akad. Lavrent'ev Avenue, Novosibirsk 630090, Russia.

PMID: 32678602
DOI: 10.1021/acs.jpcb.0c03280

Abstract

Using the method of time-resolved magnetic field effect in radiation-induced fluorescence, primary radical cations (RCs) in irradiated poly(isobutylene) (PIB) have been detected for the first time. A comparison of experimental results with the data of quantum chemical calculations suggests that the initial geometry of the ionized fragment of the PIB molecule is close to the geometry of the neutral polymer in the trans-gauche-trans-gauche conformation. The spin density of the RC in this geometry is delocalized over more than 10 polymer units, and the width of the RC's EPR spectrum is about ΔH_pp ≈ 1.3 mT. At a temperature of 273 K and lower, the lifetime of the primary RCs with the delocalized spin density exceeds 10 ns. The structural relaxation of the RCs results in the spin density localization on a single C-C bond, which is extended to nearly 0.2 nm, and in the increase in the EPR spectrum width to ΔH_pp ≈ 2.4 mT. It looks likely that this intramolecular structural relaxation is coupled strongly with those types of molecular motions that determine the process of dielectric β-relaxation in the polymer.