Zobrazeno 1 - 10
of 119
pro vyhledávání: '"Claire L, McMullin"'
Autor:
Kyle G. Pearce, Han-Ying Liu, Samuel E. Neale, Hattie M. Goff, Mary F. Mahon, Claire L. McMullin, Michael S. Hill
Publikováno v:
Nature Communications, Vol 14, Iss 1, Pp 1-5 (2023)
Abstract Counter to synthetic convention and expectation provided by the relevant standard reduction potentials, the chloroberyllate, [{SiNDipp}BeClLi]2 [{SiNDipp} = {CH2SiMe2N(Dipp)}2; Dipp = 2,6-i-Pr2C6H3)], reacts with the group 1 elements (M = Na
Externí odkaz:
https://doaj.org/article/bf8aa694578d45db8b74eaf53ae133dc
Autor:
Nathan Davison, Claire L. McMullin, Lu Zhang, Shu-Xian Hu, Paul G. Waddell, Corinne Wills, Casey Dixon, Erli Lu
Publikováno v:
Journal of the American Chemical Society. 145:6562-6576
Autor:
Nathan Davison, James A. Quirk, Floriana Tuna, David Collison, Claire L. McMullin, Hannes Michaels, George H. Morritt, Paul G. Waddell, Jamie A. Gould, Marina Freitag, James A. Dawson, Erli Lu
Publikováno v:
Davison, N, Quirk, J, Tuna, F, Collison, D, Michaels, H, Morritt, G, Waddell, P, Gould, J, Freitag, M, Dawson, J 2022, ' A room-temperature-stable electride and its reactivity: Reductive benzene/pyridine couplings and solvent-free Birch reductions ', Chem, vol. 9 . https://doi.org/10.1016/j.chempr.2022.11.006
In this work, we report the synthesis of a room-temperature-stable electride (RoSE) reagent, namely K+(LiHMDS)e− (1) (HMDS: 1,1,1,3,3,3-hexamethyldisilazide), from accessible starting materials (potassium metal and LiHMDS) via mechanochemical ball
Publikováno v:
Chemical Science. 14:2866-2876
The C–Al bond of [{SiNDipp}Al–Cu(NHCiPr)] reacts sequentially with three equivalents of terminal alkyne to provide cuprous (hydrido)(alkynyl)aluminate, (E-alkenyl)(alkynyl)aluminate and bis(alkynyl)aluminate derivatives.
Autor:
Han-Ying Liu, Samuel E. Neale, Michael S. Hill, Mary F. Mahon, Claire L. McMullin, Benjamin L. Morrison
Publikováno v:
Chemical Communications. 59:3846-3849
[{SiNDipp}MgNa]2 ({SiNDipp} = {CH2SiMe2N(Dipp)}2; Dipp = 2,6-i-Pr2C6H3) reacts directly with H2 in a process, which computational studies suggest, is dictated by the frontier MOs of both H2 and the low oxidation state s-block assembly.
Autor:
Anne-Frédérique Pécharman, Annie L. Colebatch, Michael S. Hill, Claire L. McMullin, Mary F. Mahon, Catherine Weetman
Publikováno v:
Nature Communications, Vol 8, Iss 1, Pp 1-7 (2017)
Organoboranes are widely employed in organic synthesis and typically are prepared using electrophilic boron sources. Here the authors report a route to nucleophilic boryl anions via organomagnesium-driven cleavage of boron-boron bonds.
Externí odkaz:
https://doaj.org/article/e8659eb09b804bfb9bf50536728eb2fe
Autor:
Connie J. Isaac, Fedor M. Miloserdov, Anne-Frédérique Pécharman, John P. Lowe, Claire L. McMullin, Michael K. Whittlesey
Publikováno v:
Organometallics. 41:2716-2730
Autor:
Thomas X. Gentner, Matthew J. Evans, Alan R. Kennedy, Sam E. Neale, Claire L. McMullin, Martyn P. Coles, Robert E. Mulvey
Publikováno v:
Gentner, T, Evans, M, Kennedy, A, Neale, S, McMullin, C, Coles, M & Mulvey, R 2022, ' Rubidium and caesium aluminyls: synthesis, structures and reactivity in C–H bond activation of benzene ', Chemical communications (Cambridge, England), vol. 58, no. 9, pp. 1390-1393 . https://doi.org/10.1039/D1CC05379E
Expanding knowledge of low valent aluminium chemistry, rubidium and caesium aluminyls are reported to complete the group 1 (Li–Cs) set of metal aluminyls. Both compounds crystallize as a contacted dimeric pair supported by M⋯π(arene) interaction
Autor:
Matthew J. Evans, Mathew D. Anker, Claire L. McMullin, Samuel E. Neale, Nasir A. Rajabi, Martyn P. Coles
Publikováno v:
Chemical Science. 13:4635-4646
Reaction of Al–E (E = S, Se) multiple bonds with CO functionalities generates new C–E bonds.
Autor:
Matthew J. Evans, George H. Iliffe, Samuel E. Neale, Claire L. McMullin, J. Robin Fulton, Mathew D. Anker, Martyn P. Coles
Publikováno v:
Chemical Communications. 58:10091-10094
We confirm that the μ-oxo species (NONDipp)Al(μ-O)M(BDIMes) are viable intermediates in the conversion of CO2 to carbonate promoted by bimetallic Al–Mg and Al–Zn compounds.