m-Quinone Methides fromm-Hydroxy-1,1-Diaryl Alkenes via Excited-State (Formal) Intramolecular Proton Transfer Mediated by a Water Trimer

1998 ◽  
Vol 120 (11) ◽  
pp. 2680-2681 ◽  
Author(s):  
Maike Fischer ◽  
Peter Wan
2011 ◽  
Vol 89 (3) ◽  
pp. 433-440 ◽  
Author(s):  
Matthew Lukeman ◽  
Misty-Dawn Burns ◽  
Peter Wan

1-Hydroxypyrene (1) shows unusual acid–base chemistry in its singlet excited state. Whereas most hydroxyarenes experience a marked enhancement in their acidity when excited, and rapidly deprotonate to give the corresponding phenolate anion, this is not an important pathway for 1, despite theoretical predictions that 1 should experience enhanced acidity as well. In this work, we demonstrate that 1 undergoes a competing excited state intramolecular proton transfer from the OH to carbon atoms at the 3, 6, and 8 positions of the pyrene ring to give quinone methide intermediates. When the reaction is carried out in D2O, reversion of these quinone methides to starting material results in replacement of the ring hydrogens with deuterium, providing a convenient handle to follow the reaction with NMR spectroscopy and mass spectrometry. The quantum yield for the reaction is 0.025 and appears to not be strongly dependent on the water content when aqueous acetonitrile solutions are used. 1-(2-Hydroxyphenyl)pyrene (19) was prepared and studied and shows similar reactivity to 1.


2015 ◽  
Vol 17 (14) ◽  
pp. 9205-9211 ◽  
Author(s):  
Jiani Ma ◽  
Xiting Zhang ◽  
Nikola Basarić ◽  
Peter Wan ◽  
David Lee Phillips

Excited state intramolecular proton transfer from a phenol (naphthol) to a carbon atom of the adjacent aromatic ring and formation of quinone methides was studied by femtosecond time-resolved transient absorption.


2012 ◽  
Vol 18 (34) ◽  
pp. 10617-10623 ◽  
Author(s):  
Nikola Basarić ◽  
Nađa Došlić ◽  
Jakov Ivković ◽  
Yu-Hsuan Wang ◽  
Momir Mališ ◽  
...  

2021 ◽  
Vol 154 (18) ◽  
pp. 184107
Author(s):  
Michele Nottoli ◽  
Mattia Bondanza ◽  
Filippo Lipparini ◽  
Benedetta Mennucci

2016 ◽  
Vol 4 (16) ◽  
pp. 3599-3606 ◽  
Author(s):  
Toshiki Mutai ◽  
Tatsuya Ohkawa ◽  
Hideaki Shono ◽  
Koji Araki

The color of ESIPT luminescence of HPIP is tuned in a wide range by the introduction of aryl group(s), and thus a series of PIPs showing blue to red emission is realized.


1983 ◽  
Vol 14 (28) ◽  
Author(s):  
K. DING ◽  
S. J. COURTNEY ◽  
A. J. G. STRANDJORD ◽  
S. FLOM ◽  
D. M. FRIEDRICH ◽  
...  

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