Please use this identifier to cite or link to this item:
Title: Photolysis and thermolysis of pyridyl carbonyl azide monolayers on single-crystal platinum
Authors: Adkinson, Dana K.
Magri, David C.
Pitters, Jason L.
Griffiths, Keith
Norton, Peter R.
Workentin, Mark S.
Keywords: Photochemistry -- Research
Carbonyl compounds
Crystal whiskers
Platinum compounds
Issue Date: 2013
Publisher: Wiley-Blackwell Publishing, Inc.
Citation: Adkinson, D. K., Magri, D. C., Pitters, J. L., Griffiths, K., Norton, P. R., & Workentin, M. S. (2013). Photolysis and Thermolysis of Pyridyl Carbonyl Azide Monolayers on Single‐Crystal Platinum. Photochemistry and Photobiology, 89(5), 1020-1028.
Abstract: The photochemical and thermal reactivity of a number of acyl azide-substituted pyridine compounds, namely nicotinyl azide, isonicotinyl azide, picolinyl azide and dinicotinyl azide with investigated as saturated monolayers on a single-crystal Pt(111) surface in an ultrahigh vacuum chamber. Multilayers of the substrates exhibited a maximum rate of desorption at 270 K, above which, stable saturated monolayers formed as characterized by reflection-absorption infrared spectroscopy by observation of C=O and N3 bands at 1700 cm1 , and 2100 and 1300 cm1 respectively. The monolayers were stable up to 400 K. Photolysis of the monolayer (or heating above 400 K) results in the formation of the respective isocyanate intermediate after loss of nitrogen as evidenced by the appearance of a new infrared band at 2260 cm1 with concomitant loss of the azide bands. The resulting isocyanate saturated monolayer is stable in absence of nucleophiles, but can be quenched with appropriate nucleophiles.
Appears in Collections:Scholarly Works - FacSciChe

Files in This Item:
File Description SizeFormat 
  Restricted Access
610.73 kBAdobe PDFView/Open Request a copy

Items in OAR@UM are protected by copyright, with all rights reserved, unless otherwise indicated.