Zobrazeno 1 - 10
of 372
pro vyhledávání: '"H. Cerfontain"'
Publikováno v:
ChemInform. 22
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a7a1692e8739e9355cc6e01eb0cde325
https://doi.org/10.1002/chin.199121041
https://doi.org/10.1002/chin.199121041
Autor:
B. H. Bakker, H. Cerfontain
Publikováno v:
ChemInform. 21
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f2be254bec93850c4e433da99f14d32b
https://doi.org/10.1002/chin.199020118
https://doi.org/10.1002/chin.199020118
Autor:
F. Stunnenberg, H. Cerfontain
Publikováno v:
The Journal of Physical Chemistry. 91:6490-6496
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c6752d2826c0168ca2c3b6e757259adc
https://doi.org/10.1021/j100310a014
https://doi.org/10.1021/j100310a014
Publikováno v:
Journal of the American Chemical Society. 76:4525-4534
The isotope dilution method has been employed to determine isomer distributions in the nitration of chloro-, bromo- and iodobenzenes and the relative reactivity of iodobenzene with respect to benzene. For nitration at 25o, the following isomer distri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::898e6b3a01cc452ec96f24770d6a8dd7
https://doi.org/10.1021/ja01647a005
https://doi.org/10.1021/ja01647a005
Publikováno v:
Canadian Journal of Chemistry. 49:152-156
The mechanism of sulfonation of 4-hydroxyazobenzene and of 4-hydroxyazobenzene-4′-sulfonic acid in concentrated sulfuric acid media is examined through rate correlations and comparison is drawn with sulfonation of alkyl- and halogenobenzenes by mea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a6180a42ad038f756273c78f14392eb5
https://doi.org/10.1139/v71-024
https://doi.org/10.1139/v71-024
Autor:
K. O. Kutschke, H. Cerfontain
Publikováno v:
Canadian Journal of Chemistry. 36:344-353
The photolysis of azoethane at λ 3660 Å has been reinvestigated. The quantum yield of nitrogen formation was found to be dependent on the azoethane pressure and the temperature, indicating collisional deactivation of excited azoethane molecules.The
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f852d7713af2d04d16b60e4087ebfac6
https://doi.org/10.1139/v58-049
https://doi.org/10.1139/v58-049
Autor:
K. O. Kutschke, H. Cerfontain
Publikováno v:
Journal of the American Chemical Society. 84:4017-4025
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6d43408c823e04a2782b93316db2beab
https://doi.org/10.1021/ja00880a008
https://doi.org/10.1021/ja00880a008
Publikováno v:
Physica. 19:385-390
Synopsis The radioactive decay of 112Pd → 112Ag → 112Cd has been investigated both with a βγ-coincidence apparatus and with a single channel Nal (Tl) scintillation spectrometer. A short description of the main features of the instruments is giv
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::42f86ddb567c767ff464af7a2cfe21f5
https://doi.org/10.1016/s0031-8914(53)80042-x
https://doi.org/10.1016/s0031-8914(53)80042-x
Publikováno v:
Synthetic Communications. 2:125-128
A very recent publication by Guillaud, Pierre and Arnaud 1 on the preparation and reactivity in basic media of some cyclopropyl conjugated 1,2-diketones prompted us to report our synthetic results in the same field. In connection with our interest in
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::19b6f5cba35269c848f357f3355b3865
https://doi.org/10.1080/00397917208081753
https://doi.org/10.1080/00397917208081753
Publikováno v:
Canadian Journal of Chemistry. 50:1574-1580
The behavior of the isomeric halogenobenzenesulfonic acids (halogen = F, Cl, and Br) in sulfuric acid was studied. In 115% H2SO4 at 25° only sulfonation takes place. Both the ortho- and para-isomers yield the 1-halogenobenzene-2,4-disulfonic acid, w
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::95a6139bd3c2c452918ceb1fc45ef82c
https://doi.org/10.1139/v72-249
https://doi.org/10.1139/v72-249