Zobrazeno 1 - 10
of 80
pro vyhledávání: '"Mateusz B, Pitak"'
Autor:
Helen M. O’Connor, Sergio Sanz, Aaron J. Scott, Mateusz B. Pitak, Wim T. Klooster, Simon J. Coles, Nicholas F. Chilton, Eric J. L. McInnes, Paul J. Lusby, Høgni Weihe, Stergios Piligkos, Euan K. Brechin
Publikováno v:
Molecules, Vol 26, Iss 3, p 757 (2021)
Three new heterometallic [CrIII8NiII6] coordination cubes of formulae [CrIII8NiII6L24(H2O)12](NO3)12 (1), [CrIII8NiII6L24(MeCN)7(H2O)5](ClO4)12 (2), and [CrIII8NiII6L24Cl12] (3) (where HL = 1-(4-pyridyl)butane-1,3-dione), were synthesised using the p
Externí odkaz:
https://doaj.org/article/76160d7d781a4f5fa6390e744b258d4b
Autor:
R. Owen Bonello, Mateusz B. Pitak, Graham J. Tizzard, Simon J. Coles, Ian A. Fallis, Simon J.A. Pope
Publikováno v:
Polyhedron. 228:116179
Five new imidazo[4,5-f]-1,10-phenanthroline based ligands (1–5) have been synthesised and characterised. The facile synthesis of 1–5 allows two regiochemical points of structural variety allowing highly conjugated and bulky aryl groups of varying
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::17cfd324a88eb8bfbacbc00ba6205765
https://doi.org/10.1016/j.poly.2022.116179
https://doi.org/10.1016/j.poly.2022.116179
Autor:
John V. Hanna, Gregory J. Rees, Stephen Day, Kristian E. Barnsley, Peter Gierth, Jonathan R. Yates, Simon J. Coles, Mark E. Smith, Alberth Lari, John D. Wallis, Mateusz B. Pitak
Publikováno v:
Angewandte Chemie (International Ed. in English)
A combination of charge density studies and solid state nuclear magnetic resonance (NMR) 1 J NC coupling measurements supported by periodic density functional theory (DFT) calculations is used to characterise the transition from an n–π* interactio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b9efc1479b4045c4761f8f772484cb41
https://eprints.soton.ac.uk/451693/
https://eprints.soton.ac.uk/451693/
Autor:
Simon J. Coles, Manuel E. Minas da Piedade, Hugo Meekes, Carlos Bernades, Mateusz B. Pitak, Ernst R. H. van Eck, Leyla-Cann Sögütoglu, Marina Carravetta, Terry L. Threlfall, Mike Podmore, René R. E. Steendam, Tobian A. H. de Ruiter
Publikováno v:
Crystal Growth & Design, 19, 2, pp. 907-917
Crystal Growth & Design, 19, 907-917
Crystal Growth & Design, 19, 907-917
The solid forms of acetaldehyde phenylhydrazone were investigated in detail over a century ago, with curious results: it was reported that a low melting form could be transformed into a high melting form by trace alkali, and the reverse process could
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c674c9bec610b1e52fdc2effd4516c70
https://doi.org/10.1021/acs.cgd.8b01459
https://doi.org/10.1021/acs.cgd.8b01459
Autor:
Stergios Piligkos, Priyanka Comar, Amgalanbaatar Baldansuren, Sergio Sanz, Nicholas F. Chilton, Helen M. O'Connor, Høgni Weihe, Paul J. Lusby, Eric J. L. McInnes, Mateusz B. Pitak, Simon J. Coles, Euan K. Brechin
Publikováno v:
Inorganic Chemistry. 57:3500-3506
The reaction of the simple metalloligand [FeIIIL3] [HL = 1-(4-pyridyl)butane-1,3-dione] with a variety of different MII salts results in the formation of a family of heterometallic cages of formulae [FeIII8PdII6L24]Cl12 (1), [FeIII8CuII6L24(H2O)4Br4]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4e644d2ec12a0db09227355c7ed282d4
https://doi.org/10.1021/acs.inorgchem.7b02674
https://doi.org/10.1021/acs.inorgchem.7b02674
Publikováno v:
European Journal of Inorganic Chemistry. 2017:1464-1471
The synthesis and characterisation of complexes formed from lanthanide trifluoromethanesulfonates [Ln(OTf)3] and tricyclohexylphosphine oxide (Cy3PO) or tri‐tert‐butylphosphine oxide (tBu3PO) are described. The structures of [Ln(H2O)5(Cy3PO)2]·2
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f28df135135044d969db3d8872b7dda3
https://doi.org/10.1002/ejic.201601471
https://doi.org/10.1002/ejic.201601471
Publikováno v:
European Journal of Organic Chemistry. 2017:719-725
A method for the synthesis of pyridine derivativesbased on a triple cascade reaction catalyzed by chiral secondaryamines was developed. The resulting cyclohexenes (three C–C bonds were formed) were obtained in good yields with good diastereoselecti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d99cb374535f94f683f9eee97a0b8681
https://doi.org/10.1002/ejoc.201601491
https://doi.org/10.1002/ejoc.201601491
Autor:
Richard J. Darton, William G. Marshall, John Clews, William Miller, Mateusz B. Pitak, Kevin S. Knight, Simon J. Coles, Richard H. Jones
Publikováno v:
CrystEngComm. 19:5194-5201
The structure of the complex formed between trimethylamine and iodine monochloride had been redetermined by a combination of neutron powder diffraction and X-ray single crystal diffraction techniques. The structure determined using NPD shows that the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2e0b672a88d644ad0cc1cac5d0bb71b2
https://doi.org/10.1039/c7ce00869d
https://doi.org/10.1039/c7ce00869d
Autor:
Alan R. Bassindale, Martin A. Birchall, Youssef El Aziz, Peter G. Taylor, James Bowen, Simon J. Coles, Nazia Mehrban, Mateusz B. Pitak
Publikováno v:
RSC Advances. 7:37474-37477
A novel alkyne-terminated cubic-octameric POSS was synthesised in high yield (82–90%). The X-ray crystal structure revealed intra- and intermolecular hydrogen bonding between the amide groups of the arms. Hybrid biomaterials were synthesised in nea
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::160107cd091ba83d67c974c3f5116ba7
https://doi.org/10.1039/c7ra07915j
https://doi.org/10.1039/c7ra07915j
Publikováno v:
Organometallics. 35:4004-4013
The novel coordinate compounds T8[(CH2)n-EWG]8F–-18-crown-6-M+ were prepared by reaction of EWG-(CH2)n-Si(OEt)3 (where n = 1–3 and the electron-withdrawing group, EWG, contains an Si–C(sp3) bond) with an 18-crown-6-M+F– complex (where M+ is K
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::93c668f3c19c5b4e0faeab3673ee56ef
https://doi.org/10.1021/acs.organomet.6b00565
https://doi.org/10.1021/acs.organomet.6b00565