Competing photodehydration and excited-state intramolecular proton transfer (ESIPT) in adamantyl derivatives of 2-phenylphenols

2011 ◽  
Vol 89 (2) ◽  
pp. 221-234 ◽  
Author(s):  
Nikola Basarić ◽  
Nikola Cindro ◽  
Yunyan Hou ◽  
Ivana Žabčić ◽  
Kata Mlinarić-Majerski ◽  
...  
Keyword(s):  
Excited State ◽  
Carbon Atom ◽  
Proton Transfer ◽  
Phenyl Ring ◽  
Flash Photolysis ◽  
Laser Flash Photolysis ◽  
Laser Flash ◽  
Intramolecular Proton Transfer ◽  
Hydroxyl Group ◽  
Quantum Yields

2-Phenylphenol derivatives strategically substituted with a hydroxyadamantyl substituent were synthesized and their photochemical reactivity was investigated. Derivatives 9 and 10 undergo competitive excited-state intramolecular proton transfer (ESIPT) from the phenol to the carbon atom of the adjacent phenyl ring and formal ESPT from the phenol to the hydroxyl group coupled with dehydration. These two processes (both via S1) give rise to two classes of quinone methides (QMs) that revert to starting material or react with nucleophiles, respectively. ESIPT to carbon atoms was studied by performing photolyses in the presence of D2O, whereupon deuterium incorporation to the adjacent phenyl ring was observed ([Formula: see text] = 0.1–0.2). The competing formal ESPT and dehydration takes place with quantum yields that are an order of magnitude lower and was studied by isolation of photomethanolysis products. Derivative 8 did not undergo ESIPT to carbon atom. Owing to the presence of an intramolecular H bond, an efficient ESIPT from the phenol to the hydroxyl group coupled with dehydration gives a QM that efficiently undergoes electrocyclization (overall [Formula: see text] = 0.33), to give chroman 16. In addition, spiro[adamantane-2,9′-(4′-hydroxy)fluorene] (12) undergoes ESIPT, unlike the previously reported unreactive parent 2-hydroxyfluorene. The reactive singlet excited states of the prepared biphenyl and fluorene molecules were characterized by fluorescence spectroscopy, whereas laser flash photolysis (LFP) was performed to characterize the longer lived QM intermediates.

Mechanistic studies of photohydration of m-hydroxy-1,1-diaryl alkenes

2002 ◽  
Vol 80 (1) ◽  
pp. 46-54 ◽  
Author(s):  
John G Cole ◽  
Peter Wan
Keyword(s):  
Excited State ◽  
Proton Transfer ◽  
Flash Photolysis ◽  
Laser Flash Photolysis ◽  
Parent Compound ◽  
Laser Flash ◽  
Intramolecular Proton Transfer ◽  
Quinone Methide ◽  
Quantum Yields ◽  
Nanosecond Laser

The photohydration of a variety of m-hydroxy-1,1-diaryl alkenes (8–10) and related systems (11 and 12) has been studied in aqueous CH3CN solution. All of these alkenes photohydrate efficiently in 1:1 H2O–CH3CN, to give the corresponding 1,1-diarylethanol (Markovnikov addition) products with high chemical and quantum yields. The aim of this study was to further probe the mechanism of photohydration reported for the parent m-hydroxy-α-phenylstyrene (5), which has been proposed as consisting of a water trimer-mediated excited state (formal) intramolecular proton transfer (ESIPT) from the phenolic proton to the β-carbon of the alkene moiety to give an observable (by laser flash photolysis (LFP)) m-quinone methide intermediate 6. For this purpose, derivatives of 5 with substituents (methyl or methoxy) on the α-phenyl ring as well as related model compounds were explored. Product studies, quantum yields, fluorescence, and nanosecond laser flash data are reported that are consistent with two distinct mechanisms for photohydration of these compounds: one involving water-mediated ESIPT (8, 9), as observed for the parent compound 5, and one involving direct protonation of the β-carbon by solvent water (11 and 12), with compound 10 possibly operating via both mechanisms.Key words: photohydration, solvent-assisted excited state intramolecular proton transfer (ESIPT), m-quinone methide, diarylmethyl carbocation.

Photogeneration of 1,5-naphthoquinone methides via excited-state (formal) intramolecular proton transfer (ESIPT) and photodehydration of 1-naphthol derivatives in aqueous solution

2004 ◽  
Vol 82 (2) ◽  
pp. 240-253 ◽  
Author(s):  
Matthew Lukeman ◽  
Duane Veale ◽  
Peter Wan ◽  
V Ranjit N. Munasinghe ◽  
John ET Corrie
Keyword(s):  
Aqueous Solution ◽  
Excited State ◽  
Proton Transfer ◽  
Flash Photolysis ◽  
Laser Flash Photolysis ◽  
Intramolecular Proton Transfer ◽  
Photochemical Reactions ◽  
Quinone Methide ◽  
Phenol Derivatives ◽  
Naphthol Derivatives

The photochemistry of naphthols 1, 2, 4, 5 and 9, and phenol 10 has been studied in aqueous solution with the primary aim of exploring the viability of such compounds for naphthoquinone and quinone methide photogeneration, along the lines already demonstrated by our group for phenol derivatives. 1-Naphthol (1) is known to be substantially more acidic than 2-naphthol (2) in the singlet excited state (pKa* = 0.4 and 2.8, respectively) and it was expected that this difference in excited-state acidity might be manifested in higher reactivity of 1-naphthol derivatives for photochemical reactions requiring excited-state naphtholate ions, such as quinone methide formation. Our results show that three types of naphthoquinone methides (26a, 26b, and 27) are readily photogenerated in aqueous solution by irradiation of 1-naphthols. Photolysis of the parent 1-naphthol (1) in neutral aqueous solution gave 1,5-naphthoquinone methide 26a as well as the non-Kekulé 1,8-naphthoquinone methide 26b, both via the process of excited-state (formal) intramolecular proton transfer (ESIPT), based on the observation of deuterium exchange at the 5- and 8-positions, respectively, on photolysis in D2O–CH3CN. A transient assignable to the 1,5-naphthoquinone methide 26a was observed in laser flash photolysis experiments. The isomeric 2-naphthol (2) was unreactive under similar conditions. The more conjugated 1,5-naphthoquinone methide 27 was formed efficiently via photodehydroxylation of 4; isomeric 5 was unreactive. The efficient photosolvolytic reaction observed for 4 opens the way to design related naphthol systems for application as photoreleasable protecting groups by virtue of the long-wavelength absorption of the naphthalene chromophore.Key words: photosolvolysis, excited-state intramolecular proton transfer, quinone methide, photorelease, photoprotonation.

Photophysics of Tungsten and Molybdenum Arylcarbyne Complexes. Observation of the Lowest Excited State by Laser Flash Photolysis

1996 ◽  
Vol 35 (26) ◽  
pp. 7769-7775 ◽  
Author(s):  
Thomas K. Schoch ◽  
Andrea D. Main ◽  
Richard D. Burton ◽  
Lucian A. Lucia ◽  
Edward A. Robinson ◽  
...  
Keyword(s):  
Excited State ◽  
Flash Photolysis ◽  
Laser Flash Photolysis ◽  
Laser Flash

scholarly journals Nitrile-Substituted 2-(Oxazolinyl)-Phenols: Minimalistic Excited-State Intramolecular Proton Transfer (ESIPT)-Based Fluorophores

2020 ◽  
Author(s):  
Dominik Göbel ◽  
Daniel Duvinage ◽  
Tim Stauch ◽  
Boris Nachtsheim
Keyword(s):  
Excited State ◽  
Solid State ◽  
Proton Transfer ◽  
Density Functional ◽  
Intramolecular Proton Transfer ◽  
Crystal Structure Analysis ◽  
Quantum Yields ◽  
Functional Theory ◽  
Emission Properties ◽  
Emission Enhancement

Herein, we present minimalistic single-benzene, excited-state intramolecular proton transfer (ESIPT) based fluorophores as powerful solid state emitters. The very simple synthesis gave access to all four regioisomers of nitrile-substituted 2(oxazolinyl)phenols (MW = 216.1). In respect of their emission properties they can be divided into aggregation-induced emission enhancement (AIEE) luminophores (1-CN and 2-CN), dual state emission (DSE) emitters (3-CN) and aggregation-caused quenching (ACQ) fluorophores (4‐CN). Remarkably, with compound 1-CN we discovered a minimalistic ESIPT based fluorophore with extremely high quantum yield in the solid state ΦF = 87.3% at λem = 491 nm. Furthermore, quantum yields in solution were determined up to ΦF = 63.0%, combined with Stokes shifts up till 11.300 cm–1. Temperature dependent emission mapping, crystal structure analysis and time-dependent density functional theory (TDDFT) calculations gave deep insight into the origin of the emission properties.<br>

Laser flash photolysis studies of the formation and reactivities of phenyl(naphthyl)methyl carbocations generated from phosphonium salt precursors

1992 ◽  
Vol 70 (6) ◽  
pp. 1784-1794 ◽  
Author(s):  
E. O. Alonso ◽  
L. J. Johnston ◽  
J. C. Scaiano ◽  
V. G. Toscano
Keyword(s):  
Rate Constants ◽  
Phosphonium Salt ◽  
Flash Photolysis ◽  
Laser Flash Photolysis ◽  
Ion Pairs ◽  
Laser Flash ◽  
Product Formation ◽  
Quantum Yields ◽  
Back Reaction ◽  
Transient Experiments

The photolysis of several substituted phenyl(naphthyl)methyl triphenylphosphonium chlorides has been examined using a combination of laser flash photolysis experiments and product studies. Both carbocation and radical intermediates have been characterized in the transient experiments, with the relative yields depending strongly on the solvent. For example, in alcohols, acetonitrile, or aqueous solvents cation formation predominates while acetonitrile/dioxane mixtures (5–10%) are required for the observation of radicals. Quantum yields for cation formation vary from 0.79 in methanol to 0.093 in 1:4 acetonitrile/dioxane, as measured by product studies and transient experiments, respectively. The addition of perchlorate salts leads to dramatic enhancements in the cation lifetimes; the effects are particularly pronounced for acetonitrile/dioxane mixtures where the cation yields also increase by factors of 3–4. In this case the effects are attributed primarily to replacement of chloride by perchlorate in the initial ion pairs. The combined data from both solvent and perchlorate salt effects on the cation lifetimes and yields suggest that the excited state of the phosphonium salt cleaves homolytically, followed by electron transfer within the initial radical/triphenylphosphine radical cation pair to generate carbocation, as opposed to direct heterolytic cleavage. The cation yields also indicate that back reaction to regenerate starting material, as well as product formation within the initial geminate cage, occur in some solvents. The effects of solvent and added perchlorate salts on the rate constants for reaction with nucleophiles have been examined. For example, rate constants that vary by an order of magnitude have been measured for quenching by azide ion in various aqueous acetonitrile and trifluoroethanol mixtures.

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