Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Alasdair Formanuik"'
Autor:
Alasdair Formanuik, Fabrizio Ortu, Iñigo J. Vitorica-Yrezabal, Floriana Tuna, Eric J. L. McInnes, Louise S. Natrajan, David P. Mills
Publikováno v:
Inorganics, Vol 9, Iss 12, p 86 (2021)
Tripodal multidentate ligands have become increasingly popular in f-element chemistry for stabilizing unusual bonding motifs and supporting small molecule activation processes. The steric and electronic effects of ligand donor atom substituents have
Externí odkaz:
https://doaj.org/article/65c9597e519b46c69572de28fa5ab374
Autor:
Floriana Tuna, Fabrizio Ortu, Iñigo J. Vitorica-Yrezabal, Eric J. L. McInnes, Louise S. Natrajan, David P. Mills, Alasdair Formanuik
Publikováno v:
Inorganics, Vol 9, Iss 86, p 86 (2021)
Inorganics; Volume 9; Issue 12; Pages: 86
Inorganics; Volume 9; Issue 12; Pages: 86
Tripodal multidentate ligands have become increasingly popular in f-element chemistry for stabilizing unusual bonding motifs and supporting small molecule activation processes. The steric and electronic effects of ligand donor atom substituents have
Autor:
Alasdair Formanuik, Stephen T. Liddle, Victoria E. J. Berryman, Ashley J. Wooles, Annabel R. Basford, John A. Seed, David P. Mills, Nikolas Kaltsoyannis, Benjamin L. L. Réant
We report the synthesis and characterisation of isostructural thorium(IV)- and uranium(IV)- silanide complexes, providing the first structurally authenticated Th-Si bond and a rare example of a molecular U-Si bond. These complexes therefore present t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6fb4d53d9f804963429935d1406185ac
https://doi.org/10.26434/chemrxiv.12732137
https://doi.org/10.26434/chemrxiv.12732137
Autor:
Fabrizio Ortu, Daniel Packer, Jingjing Liu, Matthew Burton, Alasdair Formanuik, David P. Mills
Publikováno v:
Journal of Organometallic Chemistry. 857:45-51
The lanthanide borohydrides [Ln(BH4)3(THF)n] [Ln = La, n = 4 (1); Ln = Ce, n = 3.5] were treated with the substituted cyclopentadienyl potassium transfer agents KCptt (Cptt = C5H3tBu2-1,3), KCpttt (Cpttt = C5H2tBu3-1,2,4) and KCp′′′ (Cp′′
Autor:
Fabrizio Ortu, Nicholas F. Chilton, David P. Mills, Jingjing Liu, Matthew Burton, Marie-Emmanuelle Boulon, Jonathan M. Fowler, Alasdair Formanuik
Publikováno v:
Ortu, F, Liu, J, Burton, M, Fowler, J M, Formanuik, A, Boulon, M-E, Chilton, N & Mills, D 2017, ' Analysis of Lanthanide-Radical Magnetic Interactions in Ce(III) 2,2′-Bipyridyl Complexes ', Inorganic Chemistry, vol. 56, no. 5, pp. 2496–2505 . https://doi.org/10.1021/acs.inorgchem.6b02683
A series of lanthanide complexes bearing organic radical ligands, [Ln(CpR)2(bipy·–)] [Ln = La, CpR = Cptt (1); Ln = Ce, CpR = Cptt (2); Ln = Ce, CpR = Cp″ (3); Ln = Ce, CpR = Cp‴ (4)] [Cptt = {C5H3tBu2-1,3}−; Cp″ = {C5H3(SiMe3)2-1,3}−; C
Autor:
Fernande Grandjean, Philip P. Power, Chun Yi Lin, Gary J. Long, Alasdair Formanuik, James C. Fettinger, Nicholas F. Chilton
Publikováno v:
Chemical Communications. 51:13275-13278
The structural and magnetic data for the Mn(i) dialkyl anionic salts [K2(18-crown-6)3][Mn{C(SiMe3)3}2]2 and [K(15-crown-5)2][Mn{C(SiMe3)3}2] are presented, indicating that these complexes possess a non-degenerate S = 2 ground state owing to 4s–3dz2
Autor:
Fabrizio Ortu, Andrew Kerridge, Eric J. L. McInnes, Ana-Maria Ariciu, Floriana Tuna, David P. Mills, Alasdair Formanuik, Reece Beekmeyer
Publikováno v:
Formanuik, A, Ariciu, A-M, Ortu, F, Beekmeyer, R, Kerridge, A, Tuna, F, Mcinnes, E & Mills, D 2016, ' Actinide covalency measured by pulsed electron paramagnetic resonance spectroscopy ', Nature Chemistry, vol. 9, pp. 578-583 . https://doi.org/10.1038/nchem.2692
Our knowledge of actinide chemical bonds lags far behind our understanding of the bonding regimes of any other series of elements. This is a major issue given the technological as well as fundamental importance of f-block elements. Some key chemical
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0e817d223027a09b2a7949e612efa899
https://doi.org/10.1038/nchem.2692
https://doi.org/10.1038/nchem.2692
Thorium(IV) alkyl synthesis from a thorium(III) cyclopentadienyl complex and an Nheterocyclic olefin
Autor:
David P. Mills, Ashley J. Wooles, John A. Seed, Jingjing Liu, Stephen T. Liddle, Fabrizio Ortu, Alasdair Formanuik
Publikováno v:
Liu, J, Seed, J, Formanuik, A, Ortu, F, Wooles, A, Mills, D & Liddle, S 2017, ' Thorium(IV) alkyl synthesis from a thorium(III) cyclopentadienyl complex and an Nheterocyclic olefin ', Journal of Organometallic Chemistry . https://doi.org/10.1016/j.jorganchem.2017.08.015
Treatment of the tris(cyclopentadienyl) thorium(III) complex [Th(η5-Cp′′)3] [1, Cp′′ = C5H3-1,3-(SiMe3)2] with the N-heterocyclic olefin H2C=C(NMeCH)2 (2) reproducibly produces the thorium(IV)-methyl derivative [Th(η5-Cp′′)3(Me)] (3) al
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3f9207ff8794cb2ffb5d875dfbf072d
https://doi.org/10.1016/j.jorganchem.2017.08.015
https://doi.org/10.1016/j.jorganchem.2017.08.015
Autor:
David P. Mills, Jingjing Liu, Floriana Tuna, Fabrizio Ortu, Alasdair Formanuik, Lydia E. Nodaraki, Andrew Kerridge
Publikováno v:
Formanuik, A, Ortu, F, Liu, J, Nodaraki, L, Tuna, F, Kerridge, A & Mills, D 2017, ' Double Reduction of 4,4′-Bipyridine and Reductive Coupling of Pyridine by Two Thorium(III) Single-Electron Transfers ', Chemistry: A European Journal, vol. 23, no. 10, pp. 2290-2293 . https://doi.org/10.1002/chem.201605974
The redox chemistry of uranium is burgeoning and uranium(III) complexes have been shown to promote many interesting synthetic transformations. However, their utility is limited by their reduction potentials, which are smaller than many non-traditiona
Autor:
Alasdair, Formanuik, Fabrizio, Ortu, Christopher J, Inman, Andrew, Kerridge, Ludovic, Castro, Laurent, Maron, David P, Mills
Publikováno v:
Chemistry (Weinheim an Der Bergstrasse, Germany)
Improving our comprehension of diverse CO2 activation pathways is of vital importance for the widespread future utilization of this abundant greenhouse gas. CO2 activation by uranium(III) complexes is now relatively well understood, with oxo/carbonat