Zobrazeno 1 - 10
of 46
pro vyhledávání: '"Brooke L. Small"'
Autor:
Brooke L. Small, Matthew F. Milner
Publikováno v:
Organometallics. 41:3320-3331
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fe68010ee0be822ea1d929910a9aad27
https://doi.org/10.1021/acs.organomet.2c00285
https://doi.org/10.1021/acs.organomet.2c00285
Publikováno v:
Reaction Kinetics, Mechanisms and Catalysis. 130:591-616
Kinetics for the reaction between 1-tetradecene and heptanoic acid to make tetradecyl heptanoates on dry Amberlyst® 15 catalyst at 90 °C are extremely complex. Observed kinetics of simultaneous double bond isomerization and esterification cannot be
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5efa225677f9664eb78d1358c9aa1ffc
https://doi.org/10.1007/s11144-020-01794-9
https://doi.org/10.1007/s11144-020-01794-9
Publikováno v:
The Journal of Physical Chemistry C. 123:3727-3739
Molecular, Fe-catalyzed ethylene oligomerization provides access to a range of linear α-olefins (LAOs) that are used to produce polyethylene, lubricants, surfactants, and other commercial products. This work provides an experimental example of an Fe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eacf501fda9d44f5ec0ba1dedca422c8
https://doi.org/10.1021/acs.jpcc.9b00129
https://doi.org/10.1021/acs.jpcc.9b00129
Autor:
Nathan Morgan, Steven M. Maley, Doo-Hyun Kwon, Michael S. Webster-Gardiner, Brooke L. Small, Orson L. Sydora, Steven M. Bischof, Daniel H. Ess
Publikováno v:
Journal of Organometallic Chemistry. 961:122251
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c83a7e6a4ca0b654ff0d8eb879cdb550
https://doi.org/10.1016/j.jorganchem.2021.122251
https://doi.org/10.1016/j.jorganchem.2021.122251
Publikováno v:
Organometallics. 34:1307-1320
Cobalt(II) dichloride complexes supported by a variety of neutral, tridentate pincer ligands have been prepared and, following in situ activation with NaBEt3H, evaluated for the catalytic borylation of 2-methylfuran, 2,6-lutidine, and benzene using b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::87dcd70a1d789e794ec5ac7130573cda
https://doi.org/10.1021/acs.organomet.5b00044
https://doi.org/10.1021/acs.organomet.5b00044
Autor:
Mark Stradiotto, Adam J. Ruddy, Sarah M. Crawford, Orson L. Sydora, Laura Turculet, Craig A. Wheaton, Colin M. Kelly, Brooke L. Small
Publikováno v:
Organometallics. 32:5581-5588
The synthesis and structural characterization of three-coordinate iron(II) and cobalt(II) complexes supported by new N-phosphinoamidinate ligands is reported, along with the successful application of these complexes as precatalysts for the challengin
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6704837b6d345ad4a9d5e6e1c14dcb5
https://doi.org/10.1021/om400883u
https://doi.org/10.1021/om400883u
Publikováno v:
Journal of Physical Organic Chemistry. 25:1409-1417
A new mechanism for the origin of multiple skeletal isomers observed in the cationic dimerization of 1-decene is proposed, and products that should form based on this mechanism are predicted. A protonated cyclopropyl intermediate appeared to form dir
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ad53b9923fa3d4e35c5ee2eed6505585
https://doi.org/10.1002/poc.3059
https://doi.org/10.1002/poc.3059
Publikováno v:
Chemistry (Weinheim an der Bergstrasse, Germany). 22(36)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::38d06760cfe844e6bd2f91fadd5a0b95
https://pubmed.ncbi.nlm.nih.gov/25187346
https://pubmed.ncbi.nlm.nih.gov/25187346
Autor:
Brooke L. Small, Michael J. Carney, Alex J. Nett, Anne A. Fischer, Thomas C. Jones, Orson L. Sydora
Publikováno v:
ACS Catalysis. 2:2452-2455
A new family of highly active ethylene tri-/tetramerization catalysts based on N-phosphinoamidinechromium complexes has been investigated. The 1-hexene to 1-octene molar ratio can be tuned from 140 to 1.5 by varying the steric environment around the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::28f665293f3465a708e22af4b869a1f4
https://doi.org/10.1021/cs300488t
https://doi.org/10.1021/cs300488t