4.6 Article

Photocatalytic alkoxylation of benzene with 3-cyano-1-methylquinolinium ion

Journal

OPTICS EXPRESS
Volume 20, Issue 6, Pages A360-A365

Publisher

OPTICAL SOC AMER
DOI: 10.1364/OE.20.00A360

Keywords

-

Categories

Funding

  1. Ministry of Education, Culture, Sports, Science and Technology, Japan [2370014, 20108010]
  2. KOSEF/MEST through WCU, Korea [R31-2008-000-10010-0]
  3. Grants-in-Aid for Scientific Research [23750014, 20108010] Funding Source: KAKEN

Ask authors/readers for more resources

One-pot alkoxylation of benzene with alcohols occurs under photoirradiation of 3-cyano-1-methylquinolinium ion in an oxygen-saturated acetonitrile solution containing benzene and alcohols. The photocatalytic reaction mechanism was clarified by nanosecond laser flash photolysis. The photocataytic alkoxylation of benzene is initiated by photoinduced electron transfer from benzene to the singlet excited state of 3-cyano-1-methylquinolinium ion, followed by the nucleophilic addition of alcohols to benzene radical cation. In the case of photoethoxylation, the optimal product and quantum yields of ethoxybenzene were 20% and 10%, respectively. (C) 2012 Optical Society of America

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.6
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available