82259-52-7Relevant academic research and scientific papers
Estimation of self-exchange electron transfer rate constants for organic compounds from stopped-flow studies
Nelsen, Stephen F.,Ramm, Michael T.,Ismagilov, Rustem F.,Nagy, Mark A.,Trieber II, Dwight A.,Powell, Douglas R.,Chen, Xi,Gengler, Jamie J.,Qu, Qinling,Brandt, Jennifer L.,Pladziewicz, Jack R.
, p. 5900 - 5907 (1997)
Second-order rate constants k12(obsd) measured at 25 °C in acetonitrile by stopped-flow for 47 electron transfer (ET) reactions among ten tetraalkylhydrazines, four ferrocene derivatives, and three p- phenylenediamine derivatives are discussed. Marcus's adiabatic cross rate formula k12(calcd) = (k11 k22 k12f12)(1/2) , Inf12 = (In K12)(2/4) ln(k11k22/Z2) works well to correlate these data. When all k12(obsd) values are simultaneously fitted to this relationship, best-fit self-exchange rate constants, k(ii)(fit), are obtained that allow remarkably accurate calculation of k12(obsd); k12(obsd)lk12'(calcd) is in the range of 0.55-1.94 for all 47 reactions. The average ΔΔG(ii)≠ between observed activation free energy and that calculated using k(ii)(fit) is 0.13 kcal/mol. Simulations using Jortner vibronic coupling theory to calculate k12 using parameters which produce the wide range of k(ii) values observed predict that Marcus's formula should be followed even when V is as low as 0.1 kcal/mol, in the weakly nonadiabatic region. Tetracyclohexyl-hydrazine has a higher k(ii) than tetraisopropylhydrazine by a factor of ca. 10. Replacing the dimethylamino groups of tetramethyl-p-phenylenediamine by 9- azabicyclo[3.3.1]nonyl groups has little effect on k(ii), demonstrating that conformations which have high intermolecular aromatic ring overlap are not necessary for large ET rate constants. Replacing a γ CH2 group of a 9- azabicyclo[3.3.1]nonyl group by a carbonyl group lowers k(ii) by a factor of 17 for the doubly substituted hydrazine and by considerably less for the doubly substituted p-phenylenediamine.
Reduction of hydrazines to amines with aqueous solution of titanium(iii) trichloride
Zhang, Yan,Tang, Qiang,Luo, Meiming
supporting information; experimental part, p. 4977 - 4982 (2011/08/05)
N-N bond cleavage in hydrazines is widely used in the preparation of amines and thus occupies a significant place in organic synthesis. In this paper, we report a new method for the reductive cleavage of N-N bonds in hydrazines by commercially available and cheap aqueous titanium(iii) trichloride. The reaction proceeds smoothly under a broad pH range from acidic to neutral and basic conditions to afford amines in good yields. This method is compatible with substrates containing functionalities such as C-C double bonds, benzyl-nitrogen bonds, benzyloxy and acyl groups. The Royal Society of Chemistry 2011.
Aza-enamines, VIII. - Electrophilic Substitution reactions at the Azomethine C-Atom of Aldehyde Dialkylhydrazones: Vilsmeier Formylation and Consecutive Reactions
Brehme, Rainer
, p. 2039 - 2046 (2007/10/02)
The reaction of hydrazones 1 with the Vilsmeier reagent yields 3-phenyl-1,4,5-triaza-1,3-pentadienium salts according to their aza-enamine character.Hydrolysis of 2 gives 1-phenylglyoxal 1-dialkylhydrazones 3, which rearrange in acidic media to 1-phenylglyoxal 2-dialkylhydrazones 4.Compound 3h forms the dihydropyrroloimidazole 5 in boiling ethanol.Pyrrolotriazinium salt 6 is obtained by the reaction of 1b with the isolated Vilsmeier reagent from dimethylformamide/oxalyl chloride.
METAL-ASSISTED REACTIONS-PART 11 RAPID REDUCTION OF N-NITROSOAMINES TO N,N-DISUBSTITUTED HYDRAZINES; THE UTILITY OF SOME LOW-VALENT TITANIUM REAGENTS
Entwistle, Ian D.,Johnstone, A. W.,Wilby, Anna H.
, p. 419 - 423 (2007/10/02)
The rapid reduction of N-nitrosoamines to N,N-disubstituted hydrazines by a low-valent titanium reagent is described.The reagent is selective in that many other functional groups are unaffected by it.The nature of the low-valent titanium reagent is discussed in terms of experimental results of comparisons of its reactivity and that of other low-valent titanium reducing agents.
