Zobrazeno 1 - 10
of 75
pro vyhledávání: '"Michael R. Gau"'
Publikováno v:
Inorganics, Vol 11, Iss 9, p 348 (2023)
Multicopper active sites for small molecule activation in materials and enzymatic systems rely on controlled but adaptable coordination spheres about copper clusters for enabling challenging chemical transformations. To translate this constrained fle
Externí odkaz:
https://doaj.org/article/8da41262f17640658d4423fade6108e3
Autor:
Grace B. Panetti, Dumitru-Claudiu Sergentu, Michael R. Gau, Patrick J. Carroll, Jochen Autschbach, Patrick J. Walsh, Eric J. Schelter
Publikováno v:
Nature Communications, Vol 12, Iss 1, Pp 1-7 (2021)
Ce(IV) organometallic compounds are rare due to Ce(IV) being a powerful oxidant. Herein, the authors explore the covalency of a pair of organocerium complexes bearing a Ce(IV)-C(aryl) bond and examine their structure by NMR spectroscopy, X-ray diffra
Externí odkaz:
https://doaj.org/article/353226de13d34f4f95d8e07ece1a0bc0
Autor:
Aislinn C. Whalen, Claudia Hernandez Brito, Kyoung H. Choi, Ellen J. T. Warner, David A. Thole, Michael R. Gau, Patrick J. Carroll, Mitchell R. Anstey
Publikováno v:
IUCrData, Vol 5, Iss 9, p x201276 (2020)
In the crystalline state of the title solvate, C18H13NO3·C4H8O, hydrogen-bonding interactions between hydroxyl groups on a phenoxazine backbone and the tetrahydrofuran solvent are observed that suggest the ability for this compound to act as a chela
Externí odkaz:
https://doaj.org/article/422707ae9e614848aa5f8f10ad369369
Autor:
Hannah H. Mallard, Nicholas D. Kennedy, Nathan A. Rudman, Alexa M. Greenwood, Jonathan Nicoleau, Corey E. Angle, Nicole A. Torquato, Michael R. Gau, Patrick J. Carroll, Mitchell R. Anstey
Publikováno v:
IUCrData, Vol 5, Iss 9, p x201248 (2020)
In the title compound, C40H36B2N4O5, the B—O—B bond angle is 132.75 (13) and the dihedral angle between the benzodiazborole rings is 73.02 (5)°. In the crystal, weak C—H...O interactions link the molecules.
Externí odkaz:
https://doaj.org/article/750cfc246cd047e9a2e3a833424cfb04
Publikováno v:
Acta Crystallographica Section E: Crystallographic Communications, Vol 74, Iss 7, Pp 918-925 (2018)
The solid-state structures of the Na+, Li+, and NH4+ salts of the 4,5-dihydroxybenzene-1,3-disulfonate (tiron) dianion are reported, namely disodium 4,5-dihydroxybenzene-1,3-disulfonate, 2Na+·C6H4O8S22−, μ-4,5-dihydroxybenzene-1,3-disulfonato-bis
Externí odkaz:
https://doaj.org/article/e22d90500e354f8e92a7ea0507514b0d
Autor:
Orion Staples, Magali S. Ferrandon, Guillaume P. Laurent, Uddhav Kanbur, A. Jeremy Kropf, Michael R. Gau, Patrick J. Carroll, Katherine McCullough, Dieter Sorsche, Frédéric A. Perras, Massimiliano Delferro, David M. Kaphan, Daniel J. Mindiola
Publikováno v:
Journal of the American Chemical Society. 145:7992-8000
Publikováno v:
Chemical Science. 14:291-297
It has been a long-standing challenge to develop organic molecular capsules for selective anion binding in water.
Publikováno v:
Dalton Transactions. 52:5909-5917
The photophysical properties and photochemical reactivity of the organometallic mono(cyclooctatetraenide)-Ce(iii) complexes: [(C8H8)Ce(μ-X)(THF)2]2 X = O3SCF3− (1), Cl− (2), were studied.
Publikováno v:
Inorganic Chemistry. 61:20785-20792
5-Methyl-2-[(2-nitrophenyl)amino]-3-thiophenecarbonitrile (ROY) is considered to be the most crystalline polymorphic organic molecule discovered to date with 12 fully characterized crystal structures present in the Cambridge Structural Database (CSD)
Publikováno v:
Organometallics. 41:3341-3348