ChemInform Abstract: Effect of Solvent on the Stability of mero-Substituted Alkyl Radicals.

ChemInform ◽  
1987 ◽  
Vol 18 (45) ◽  
Author(s):  
H.-D. BECKHAUS ◽  
C. RUECHARDT
2013 ◽  
Vol 58 (10) ◽  
pp. 1166-1171 ◽  
Author(s):  
O. A. Kapush ◽  
L. I. Trishchuk ◽  
V. N. Tomashik ◽  
Z. F. Tomashik ◽  
S. D. Boruk

2012 ◽  
Vol 10 (4) ◽  
pp. 1253-1261 ◽  
Author(s):  
Mohamed Shehate ◽  
Mohamed Shoukry ◽  
Mona Ragab

AbstractThe Pd(DMPA)Cl2 complex, where DMPA = N,N-dimethylaminoproylamine, was synthesized and characterized. The stoichiometry and stability constants of the complexes formed between various dicarboxylic acids and [Pd(DMPA)(H2O)2]2+ were investigated. The effect of solvent dielectric constant, chloride ion concentration of the medium and temperature on the stability constant of the cyclobutanedicaroxylic acid (CBDCA) complex was investigated. The equilibrium constants for the displacement of coordinated CBDCA by inosine, taken as an example of DNA constituents, were calculated. The results are expected to contribute to the chemistry of antitumour agents.


1997 ◽  
Vol 75 (8) ◽  
pp. 1055-1075 ◽  
Author(s):  
Donald R. Arnold ◽  
Kimberly A. McManus ◽  
Mary S.W. Chan

The scope of the photochemical nucleophile–olefin combination, aromatic substitution (photo-NOCAS) reaction has been extended to include cyanide anion as the nucleophile. Highest yields of adducts were obtained when the alkene or diene has an oxidation potential less than ca. 1.5 V (SCE). No adducts were obtained from 2-methylpropene (9), oxidation potential 2.6 V. Oxidation of cyanide anion, by the radical cation of the alkene or diene, can compete with the combination. With the alkenes, 2,3-dimethyl-2-butene (2) and 2-methyl-2-butene (10), both nitriles and isonitriles were obtained; isonitriles were not detected from the reactions involving the dienes, 2-methyl-1,3-butadiene (11), 2,3-dimethyl-1,3-butadiene (12), 4-methyl-1,3-pentadiene (13), 2,4-dimethyl-1,3-pentadiene (14), and 2,5-dimethyl-2,4-hexadiene (6). The specificity, nitrile versus isonitrile, is explained in terms of the Hard-Soft-Acid-Base (HSAB) principle. The photo-NOCAS reaction also occurs with the allene, 2,4-dimethyl-2,3-pentadiene (15), cyanide combining at the central carbon. Factors influencing the regiochemistry of the combination step, Markovnikov versus anti-Markovnikov, have been defined. Cyanide anion adds preferentially to the less alkyl-substituted, less sterically hindered, end of an unsymmetric alkene or conjugated diene radical cation, forming the more heavily alkyl-substituted radical intermediate. High-level abinitio molecular orbital calculations (MP2/6-31G*//HF/6-31G*) have been used to determine the effect of alkyl substitution on the stability of the intermediates, β-cyano and β-isocyano alkyl radicals, and products, alkyl cyanides and isocyanides. The more heavily alkyl-substituted radical is not necessarily the more stable. The product ratio (Markovnikov versus anti-Markovnikov) must be kinetically controlled. Keywords: photochemistry, radical ions, electron transfer, nitriles, isonitriles.


Synlett ◽  
2020 ◽  
Author(s):  
Robert J. Phipps ◽  
Barbara W. Hadrys

Minisci-type reactions comprise an important class of reactions for the direct functionalization of basic heterocyclic compounds. On certain heterocycles, such as quinolines, Minisci-type reactions face a regioselectivity choice which often results in mixtures of regioisomers at the C2 and C4 positions, limiting utility. We present a study of the effect of solvent and Brønsted acid catalyst on regioselectivity in the addition of N-acetyl-substituted, α-amino alkyl radicals to quinolines. By tuning the solvent and acid combination we identify conditions that strongly favour C2 and strongly favour C4 and present a small scope of compatible substrates.


1985 ◽  
Vol 107 (10) ◽  
pp. 2872-2880 ◽  
Author(s):  
Wing Tsang
Keyword(s):  

1974 ◽  
Vol 27 (10) ◽  
pp. 2267 ◽  
Author(s):  
NA Evans ◽  
DE Rivett ◽  
JFK Wilshire

The effect of solvent and structure on the stability to light of a series of 1,3-diphenyl-2-pyrazolines has been studied. The major photochemical reaction observed is dehydrogenation to the corresponding 1,3-diphenylpyrazole unless the 5-position is disubstituted when, as in the case of 1,3,5,5-tetraphenyl-2- pyrazoline, photo-oxidation, with either retention or destruction of the heterocyclic ring, occurs. Evidence is presented that singlet oxygen may be involved in the photodehydrogenation of 1,3- diphenyl-2-pyrazoline. The observation that the presence of bulky groups in both the 4- and 5-positions improved both the fluorescence efficiency and the stability to light of the 1,3-diphenyl-2-pyrazoline molecule may have significance for the design of pyrazoline whitening agents. Dehydrogenation of the same series of pyrazolines with chloranil has been studied in order to determine the effect of substituents on the yield of pyrazole.


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