Zobrazeno 1 - 10
of 22
pro vyhledávání: '"Bradley E. Cowie"'
Autor:
Bradley E. Cowie, Lisa Häfele, Andreas Phanopoulos, Said A. Said, Ja Kyung Lee, Anna Regoutz, Milo S. P. Shaffer, Charlotte K. Williams
This work applies organometallic routes to copper(0/I) nanoparticles and describes how to match ligand chemistries with different material compositions. The syntheses involve reacting an organo-copper precursor, mesitylcopper(I) [CuMes]z (z=4, 5), at
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::57cb56b98f0339fdf5e9302728691088
http://hdl.handle.net/10044/1/104460
http://hdl.handle.net/10044/1/104460
Publikováno v:
Cowie, B E, Porley, V & Robertson, N 2020, ' Solar Disinfection (SODIS) Provides a Much Underexploited Opportunity for Researchers in Photocatalytic Water Treatment (PWT) ', ACS Catalysis, pp. 11779-11782 . https://doi.org/10.1021/acscatal.0c03325
Publikováno v:
Chemical Science
Chemical Science, 2020, 11 (27), pp.7144-7157. ⟨10.1039/d0sc02297g⟩
Chemical Science, 2020, 11 (27), pp.7144-7157. ⟨10.1039/d0sc02297g⟩
The oxo- and catecholate-bridged UIV/UIV Pacman complex [{(py)UIVOUIV(μ-O2C6H4)(py)}(LA)] A (LA = a macrocyclic "Pacman" ligand; anthracenylene hinge between N4-donor pockets, ethyl substituents on meso-carbon atom of each N4-donor pocket) featuring
Publikováno v:
Comprehensive Coordination Chemistry III ISBN: 9780081026892
Comprehensive Coordination Chemistry III
Comprehensive Coordination Chemistry III
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4d526cad6de05185361590f1e5b56c80
https://doi.org/10.1016/b978-0-08-102688-5.00080-5
https://doi.org/10.1016/b978-0-08-102688-5.00080-5
Publikováno v:
Chemical Science
A UIV/UIV “Pacman” complex exhibits facile oxo-ligand functionalisation and substitution reactivity, owing to a bridging catecholate ligand that enhances the μ-oxo nucleophilicity and stabilises the resulting products.
The oxo- and catechol
The oxo- and catechol
Autor:
Bradley E. Cowie, David J. H. Emslie
Publikováno v:
Canadian Journal of Chemistry. 96:484-491
Reaction of [Rh(μ-Cl)(CO)(TXPB)] (1; TXPB = 2,7-di-tert-butyl-5-diphenylboryl-4-diphenylphosphino-9,9-dimethylthioxanthene) with NaBH4 yielded square planar [Rh(μ-H)(CO)(TXPB)] (2) in which the hydride ligand bridges between rhodium and the borane
Autor:
David J. H. Emslie, Bradley E. Cowie
Publikováno v:
Organometallics. 37:1007-1016
The reaction of a borane-appended analogue of 1,1′-bis(phosphino)ferrocene, [Fe(η5-C5H4PPh2)(η5-C5H4PtBu{(o-BPh2)C6H4})] (FcPPB), with [W(CO)6] under photochemical conditions lead to [W(CO)4(FcPPB*)] (1) (FcPPB* = [Fe(η5-C5H4PPh2){η5-C5H3P(tBu)
Publikováno v:
Chemical reviews. 119(18)
The uranyl ion, [U
Publikováno v:
Cowie, B E, Purkis, J M, Austin, J, Love, J B & Arnold, P L 2019, ' Thermal and Photochemical Reduction and Functionalization Chemistry of the Uranyl Dication, [U VI O2] 2+ ', Chemical Reviews . https://doi.org/10.1021/acs.chemrev.9b00048
The uranyl ion, [UVIO2]2+, possesses rigorously trans, strongly covalent, and chemically robust Uoxo groups. However, through the use of anaerobic reaction techniques, both one and two-electron reductive functionalization of the uranyl oxo groups hav
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::70a5607ccc75052b8615a2398cbf5182
https://www.pure.ed.ac.uk/ws/files/107533807/20190815_Arnold_UranylOxo_CR_MS_AAV_002_.pdf
https://www.pure.ed.ac.uk/ws/files/107533807/20190815_Arnold_UranylOxo_CR_MS_AAV_002_.pdf
Autor:
David J. H. Emslie, Bradley E. Cowie
Publikováno v:
Organometallics. 34:4093-4101
Reaction of a ferrocene-backbone bisphosphine-borane ligand, [Fe(η5-C5H4PPh2)(η5-C5H4PtBu{C6H4(BPh2)-o})] (FcPPB), with [Ni(cod)2] (cod = 1,5-cyclooctadiene) or 0.5 equiv of [Pd2(dba)3] (dba = trans,trans-dibenzylideneacetone) afforded [Ni(FcPPB)]