The photoreduction behavior of p-nitroaniline (pNA) in the presence of N,N-dimethylaniline (DMA) induced by both steady-state (365 nm) and laser (337 nm) irradiation has been analyzed. The stoichiometry of the photoreduction reaction revealed that several amino radicals derived from DMA were generat
A new photoinitiator system based on p-nitroaniline in the presence of aliphatic tertiary amines
✍ Scribed by Angel Costela; Inmaculada García-Moreno; Javier Dabrio; Roberto Sastre
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 641 KB
- Volume
- 198
- Category
- Article
- ISSN
- 1022-1352
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✦ Synopsis
Abstract
Several kinetic aspects of the polymerization of dodecyl acrylate photoinitiated with p‐nitroaniline in the presence of an aliphatic tertiary amine, either 2‐(N,N‐diethylamino)ethanol or 2‐(N,N‐dimethylamino)ethyl methacrylate, acting as coinitiator, were studied. Under low absorption conditions, the rate of polymerization was found to be proportional to the square‐root of the incident light intensity, the initiator and the coinitiator concentrations. The polymerization behaviour was analyzed also under aerobic conditions. Under identical irradiation conditions, both initiation and polymerization processes present higher rates and quantum yields than those obtained with conventional aromatic ketone photoinitiators.
📜 SIMILAR VOLUMES
Steady-state photolysis at 365 nm has been employed to carry out a structure-reactivity investigation of the 2,6-dihalogen derivatives ofp-nitroaniline (pNA). Detailed studies of the spectroscopy of these molecules were accomplished. Photoreduction behavior of the 2,6-dihalogen derivatives of p-nitr