Phototransformation of resorcinol induced by excitation of nitrite and nitrate ions. II: nitrate ions

Article abstract of DOI:10.1080/02772249409358000

The excitation of nitrate ions in an aqueous solution of resorcinol (I) at pH = 5.5-6.5, leads to a mixture of 1,2,3-trihydroxybenzene (II), 1,2,4-trihydroxybenzene (III), 4-nitrosoresorcinol (V) and 4-nitroresorcinol (VII). A secondary formation of 2, 4-dinitrosoresorcinol (VI) was also detected.

Full text of DOI:10.1080/02772249409358000

This article was downloaded by: [University of California, Berkeley]
On: 09 March 2015, At: 21:51
Publisher: Taylor & Francis
Informa Ltd Registered in England and Wales Registered Number: 1072954
Registered office: Mortimer House, 37-41 Mortimer Street, London W1T 3JH, UK
Toxicological & Environmental
Chemistry
Publication details, including instructions for authors and
subscription information:
http://www.tandfonline.com/loi/gtec20
Phototransformation of resorcinol
induced by excitation of nitrite and
nitrate ions. II: Nitrate ions
a
a
F. Machado & P. Boule
a
Laboratoire de Photochimie Moléculaire et
Macromoléculaire , URA CNRS , 433 Université Blaise Pascal
(Clermont‐Ferrand), Aubière Cedex, 63177, France
Published online: 19 Sep 2008.
To cite this article: F. Machado & P. Boule (1994) Phototransformation of resorcinol induced by
excitation of nitrite and nitrate ions. II: Nitrate ions, Toxicological & Environmental Chemistry,
42:3-4, 165-173, DOI: 10.1080/02772249409358000
To link to this article: http://dx.doi.org/10.1080/02772249409358000
PLEASE SCROLL DOWN FOR ARTICLE
Taylor & Francis makes every effort to ensure the accuracy of all the information
(
&
the “Content”) contained in the publications on our platform. However, Taylor
Francis, our agents, and our licensors make no representations or warranties
whatsoever as to the accuracy, completeness, or suitability for any purpose of the
Content. Any opinions and views expressed in this publication are the opinions and
views of the authors, and are not the views of or endorsed by Taylor & Francis. The
accuracy of the Content should not be relied upon and should be independently
verified with primary sources of information. Taylor and Francis shall not be liable
for any losses, actions, claims, proceedings, demands, costs, expenses, damages,
and other liabilities whatsoever or howsoever caused arising directly or indirectly in
connection with, in relation to or arising out of the use of the Content.
This article may be used for research, teaching, and private study purposes. Any
substantial or systematic reproduction, redistribution, reselling, loan, sub-licensing,
systematic supply, or distribution in any form to anyone is expressly forbidden.

Terms & Conditions of access and use can be found at http://www.tandfonline.com/
page/terms-and-conditions