Gas phase reactivity of the cyclohexadienyl radical with O2 and NO and thermochemistry of the association reaction with NO
Literature Information
Florence Berho, Robert Lesclaux
The kinetics of the reaction of the cyclohexadienyl radical (C6H7) with O2 and NO have been investigated for the first time using flash photolysis coupled to UV absorption spectrometry. The kinetic study was complemented by a thermochemical study of the association reaction of the C6H7 radical with NO. The reaction with O2 was found to be fairly slow, k(C6H7 + O2) = (4.0 ± 2.0) × 10−14 cm3 molecule−1 s−1 at 298 K, thus confirming the low reactivity of cyclohexadienyl-type radicals towards O2. The association reaction of C6H7 with NO is faster: k(C6H7 + NO) = (1.8 ± 0.5) × 10−12 cm3 molecule−1 s−1 (280 K, 1 atm pressure H2) and yet the rate constant is one order of magnitude smaller than the usual values observed for radical reactions with NO. RRKM calculations have indicated that pressure effects are small under these conditions, the rate constant being only 30 to 40% smaller than the high pressure limiting value. The reaction of C6H7 with NO was found to be equilibrated at T>300 K, under our experimental conditions. The equilibrium constant was measured at 4 different temperatures between 300 and 373 K, yielding the following expression: ln(Kc/cm3 molecule−1) = (−62.6 ± 1.0) + [(8680 ± 700) K/T]. A thermodynamic treatment of the data, using the Third Law method of analysis, yielded ΔH298° = − (74.9 ± 7.0) kJ mol−1, corresponding to the calculated value of ΔS298° = − (159 ± 8) J K−1 mol−1 (using AM1 calculations). This weak value of the R–NO bond dissociation energy is related to the resonance stabilisation energy of the C6H7 radical. The present results are discussed by comparison with those obtained for other cyclohexadienyl-type radicals. In particular, an explanation is suggested for the discrepancies observed in the literature concerning the kinetics of the hydroxycyclohexadienyl (HOC6H6) radical reaction with NO.
Recommended Journals
Related Literature
Dispersion interactions in silicon allotropes
Antti J. Karttunen, Denis Usvyat, Martin Schütz, Lorenzo Maschio
DOI: 10.1039/C6CP08873B
Photoelectron spectroscopy of isolated luciferin and infraluciferin anions in vacuo: competing photodetachment, photofragmentation and internal conversion
Joanne L. Woodhouse, Mariana Assmann, Michael A. Parkes, Helen Grounds, Steven J. Pacman, James C. Anderson, Graham A. Worth, Helen H. Fielding
DOI: 10.1039/C7CP04815G
Comment on “Brownian diffusion of a particle at an air/liquid interface: elastic (not viscous) response of the surface”
G. Boniello, A. Stocco, C. Blanc, M. Nobili
DOI: 10.1039/C7CP02970E
Preservation of electronic properties of double-decker complexes on metallic supports
B. Cirera, J. Matarrubia, T. Kaposi, N. Giménez-Agulló, M. Paszkiewicz, F. Klappenberger, J. V. Barth, W. Auwärter, D. Ecija
DOI: 10.1039/C6CP08239D
Formation of coronene:water complexes: FTIR study in argon matrices and theoretical characterisation
A. Simon, J. A. Noble, G. Rouaut, C. Aupetit, C. Iftner, J. Mascetti
DOI: 10.1039/C6CP08559H
Different natures of surface electronic transitions of carbon nanoparticles
A. Cayuela, M. L. Soriano, F. M. Gelardi, M. Cannas, M. Valcárcel, F. Messina
DOI: 10.1039/C7CP04548D
Ultrafast excited-state relaxation of a binuclear Ag(i) phosphine complex in gas phase and solution
S. V. Kruppa, F. Bäppler, W. Klopper, S. P. Walg, W. R. Thiel, R. Diller
DOI: 10.1039/C7CP04128D
Photoluminescence from vibrational excited-states for organic molecules adsorbed on Si nanoparticles
M. Maeda, T. Matsumoto, H. Kobayashi
DOI: 10.1039/C7CP01836C
Ferrocene and ferrocenium inclusion compounds with cucurbiturils: a study of metal atom dynamics probed by Mössbauer spectroscopy
Clara I. R. Magalhães, Ana C. Gomes, André D. Lopes, Isabel S. Gonçalves, Martyn Pillinger, Eunyoung Jin, Ikjin Kim, Young Ho Ko, Israel Nowik, Rolfe H. Herber
DOI: 10.1039/C7CP04416J
Defluorination and covalent grafting of fluorinated graphene with TEMPO in a radical mechanism
Wenchuan Lai, Dazhou Xu, Xu Wang, Zaoming Wang, Yang Liu, Xiaojiao Zhang, Yulong Li, Xiangyang Liu
DOI: 10.1039/C7CP04439A
You might also like
What are the main uses of 4-Nitrophenyl phosphate disodium salt hexahydrate (CAS: 333338-18-4)?
4-Nitrophenyl phosphate disodium salt hexahydrate is primarily used as a substra...
What are the main uses of 2-(Trifluoromethyl)-1,3-oxazole-4-carboxylic Acid (CAS: 1060816-01-4)?
2-(Trifluoromethyl)-1,3-oxazole-4-carboxylic Acid (CAS: 1060816-01-4) is widely ...
How should 2-Fluoro-4-biphenylcarboxylic acid (CAS: 137045-30-8) be stored?
2-Fluoro-4-biphenylcarboxylic acid should be stored in a cool, dry place at room...
What industries use Prednisolone-21-Carboxylic Acid (CAS: 61549-70-0)?
Prednisolone-21-Carboxylic Acid is primarily used in the pharmaceutical industry...
How should 4-(Hydrazinomethyl)-1,2,3-benzenetriol (CAS: 3614-72-0) be stored?
4-(Hydrazinomethyl)-1,2,3-benzenetriol (CAS: 3614-72-0) should be stored in a co...
What industries use 4-Amino-1-methyl-1H-pyrazole-5-carboxylic acid hydrochloride (CAS: 92534-70-8)?
4-Amino-1-methyl-1H-pyrazole-5-carboxylic acid hydrochloride (CAS: 92534-70-8) i...
What regulatory guidelines apply to dehydropachymic acid (CAS: 77012-31-8)?
Dehydropachymic acid (CAS: 77012-31-8) is regulated by various agencies. It fall...
What is the market or research trend for 6-[(2,2-Dimethylpropanoyl)amino]nicotinic acid (CAS: 898561-66-5)?
The market and research trends for 6-[(2,2-Dimethylpropanoyl)amino]nicotinic aci...
How should 1,10-Phenanthroline-2,9-dicarbaldehyde (CAS: 57709-62-3) be stored?
1,10-Phenanthroline-2,9-dicarbaldehyde should be stored in a cool, dry place awa...
How is 5-Carbamoyl-11-oxo-10,11-dihydro-5H-dibenzo[b,f]azepin-10-yl acetate (CAS: 113952-21-9) typically synthesized?
5-Carbamoyl-11-oxo-10,11-dihydro-5H-dibenzo[b,f]azepin-10-yl acetate can be synt...
Source Journal
Physical Chemistry Chemical Physics

Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.














