Zobrazeno 1 - 10
of 168
pro vyhledávání: '"J. W. Hilborn"'
Publikováno v:
Journal of the American Chemical Society. 116:3337-3346
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::1530deb939de4ff0409a3fb66a941f3a
https://doi.org/10.1021/ja00087a020
https://doi.org/10.1021/ja00087a020
Autor:
Zhidao Huang (AUTHOR), Akana, Michelle E.1 (AUTHOR), Sanders, Kyana M.1 (AUTHOR), Weix, Daniel J.1 (AUTHOR) dweix@wisc.edu
Publikováno v:
Science. 9/20/2024, Vol. 385 Issue 6715, p1331-1337. 7p. 5 Diagrams.
Autor:
J. W. Hilborn, Ronald D. Curtis, Gang Wu, James A. Pincock, Michael D. Lumsden, Roderick E. Wasylishen
Publikováno v:
The Journal of Physical Chemistry. 97:1856-1861
Nitrogen-15 NMR spectra have been obtained for spinning and static powder samples of solid cis-azobenzene- 15 N 2 (1). This nitrogen NMR spectra obtained with magic angle spinning exhibited spinning rate-dependent line shapes which are characteristic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::90c5eb344c1ee19585b3c59c841df1ff
https://doi.org/10.1021/j100111a023
https://doi.org/10.1021/j100111a023
Autor:
J. W. Hilborn, James A. Pincock
Publikováno v:
ChemInform. 22
Rates of decarboxylation (k CO2 R ) have been estimated for the acyloxy radicals formed in the photolysis of substituted 1-naphthylmethyl alkanoates. These rates are based on a proposed mechanism involving initial carbon-oxygen homolytic bond cleavag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::302f0ec2306f7ac3fc22628c3922d465
https://doi.org/10.1002/chin.199129076
https://doi.org/10.1002/chin.199129076
Autor:
James A. Pincock, J. W. Hilborn
Publikováno v:
ChemInform. 23
The photolysis of esters 6 and 8 in methanol leads to products resulting from both naphthylmethyl cations and radicals. The product distribution is nearly independent of X for the esters 6 except w...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::adf6cdb31d3b127e04d7c22ee70d08fd
https://doi.org/10.1002/chin.199247092
https://doi.org/10.1002/chin.199247092
Autor:
James A. Pincock, Ronald D. Curtis, J. W. Hilborn, Gang Wu, Michael D. Lumsden, Roderick E. Wasylishen
Publikováno v:
ChemInform. 24
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d58a85fa9c0b8aa4e27d1204a1aa7850
https://doi.org/10.1002/chin.199325041
https://doi.org/10.1002/chin.199325041
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::e0ac0ef63e2e9e81ec8a31dc9b5aba70
https://doi.org/10.1002/chin.199434080
https://doi.org/10.1002/chin.199434080
Autor:
James A. Pincock, J. W. Hilborn
Publikováno v:
Canadian Journal of Chemistry. 70:992-999
The photolysis of esters 6 and 8 in methanol leads to products resulting from both naphthylmethyl cations and radicals. The product distribution is nearly independent of X for the esters 6 except when X equals methoxy. A mechanism involving initial h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::adb6c83d8576663e2e404bca8f40f5df
https://doi.org/10.1139/v92-131
https://doi.org/10.1139/v92-131
Autor:
J. W. Hilborn, James A. Pincock
Publikováno v:
Journal of the American Chemical Society. 113:2683-2686
Rates of decarboxylation (k CO2 R ) have been estimated for the acyloxy radicals formed in the photolysis of substituted 1-naphthylmethyl alkanoates. These rates are based on a proposed mechanism involving initial carbon-oxygen homolytic bond cleavag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::40a2c639a3f603f0caa71c577290a1bc
https://doi.org/10.1021/ja00007a049
https://doi.org/10.1021/ja00007a049
Autor:
He, Jingli1 (AUTHOR), Li, Zhaodi1 (AUTHOR), Li, Ruhui1 (AUTHOR), Kou, Xuezhen2 (AUTHOR), Liu, Delong1 (AUTHOR) dlliu@sjtu.edu.cn, Zhang, Wanbin1,2 (AUTHOR) wanbin@sjtu.edu.cn
Publikováno v:
Advanced Science. 6/19/2024, Vol. 11 Issue 23, p1-12. 12p.