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The reactivity of p-nitrophenyl esters with surfactants in apolar solvents. V. p-Nitrophenyl acetate in benzene solutions of butane-1,4-diamine bis(dodecanoate)

Autor: CJ O'Conner, TD Lomax

Publikováno v: Australian Journal of Chemistry. 36:895

The rate of decomposition of p-nitrophenyl acetate in benzene in the presence of butane-1,4-diamine bis(dodecanoate) (budb) has been measured at temperatures between 333 and 353 K. The data fit a rate equation which consists of a term arising from mi

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::8f01bc802d5a416f047b54978f0417a6
https://doi.org/10.1071/ch9830895

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The reactivity of p-nitrophenyl esters with surfactants in apolar solvents. VI. Structural effects on the reaction of p-nitrophenyl acetate with alkanediamine bis(dodecanoate) salts

Autor: CJ O'Conner, TD Lomax

Publikováno v: Australian Journal of Chemistry. 36:907

The rate of decomposition of p-nitrophenyl acetate has been measured in benzene solutions of a series of alkane-α,ω-diamine bis(dodecanoate) salts. Me(CH2)10CO2-+NH3(CH2)NH3N+ -O2C(CH2)10ME(n=2-7,9,10,12) The micellar rate constant is affected by t

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::27d7250ffb79078180641c8759ac52d5
https://doi.org/10.1071/ch9830907

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The reactivity of p-nitrophenyl esters with surfactants in apolar solvents. VII. Substituent effects on the reactivity of 4'-nitrophenyl 4-substituted benzoates in benzene solutions of dodecylammonium propionate and butane-1,4-diamine bis(dodecanoate)

Autor: TD Lomax, CJ O'Conner

Publikováno v: Australian Journal of Chemistry. 36:917

The rate of decomposition of a series of 4'-nitrophenyl 4-substituted benzoates has been measured at 341 K in benzene solutions of dodecylammonium propionate and butane-1,4-diamine bis-(dodecanoate). The bimolecular rate constant due to general acid-

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::c6135cfd945853b9eae747a8356c529c
https://doi.org/10.1071/ch9830917

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Substituent effects on the N.M.R. spectra of carboxylic acid derivatives. III. Correlation of 13C N.M.R. spectra of para substituted acetanilides and 4'-nitrophenyl 4-substituted benzoates with infrared carbonyl stretching frequencies, 1H N.M.R., rate and equilibrium data

Autor: TD Lomax, CJ O'Conner, DA Rogers, AJ Porter, DJ McLennan, DJ Calvert

Publikováno v: Australian Journal of Chemistry. 37:497

The 13C n.m.r. spectra of 17 monosubstituted benzenes, 14 para substituted acetanilides and ten 4'-nitrophenyl 4-substituted benzoates have been measured in (CD3)2SO and the chemical shifts have been compared with the infrared carbonyl stretching fre

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9884b956af18a936e4c222a7042a8981
https://doi.org/10.1071/ch9840497

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Akademický článek

Tabby pattern alleles of the domestic cat.

Autor: Lomax TD; Forest Research Institute, Rotorua, New Zealand., Robinson R

Publikováno v: The Journal of heredity [J Hered] 1988 Jan-Feb; Vol. 79 (1), pp. 21-3.

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