Mix and match - controlling the functionality of spin-crossover materials through solid solutions and molecular alloys.

Autor: Halcrow MA; School of Chemistry, University of Leeds, Woodhouse Lane, Leeds, LS2 9JT, UK. m.a.halcrow@leeds.ac.uk.

Publikováno v: Dalton transactions (Cambridge, England : 2003) [Dalton Trans] 2024 Aug 20; Vol. 53 (33), pp. 13694-13708. Date of Electronic Publication: 2024 Aug 20.

A Survey of the Angular Distortion Landscape in the Coordination Geometries of High-Spin Iron(II) 2,6-Bis(pyrazolyl)pyridine Complexes.

Autor: Capel Berdiell I; School of Chemistry, University of Leeds, Woodhouse Lane, Leeds LS2 9JT, U.K., Michaels E; School of Chemistry, University of Leeds, Woodhouse Lane, Leeds LS2 9JT, U.K., Munro OQ; School of Chemistry, University of Leeds, Woodhouse Lane, Leeds LS2 9JT, U.K., Halcrow MA; School of Chemistry, University of Leeds, Woodhouse Lane, Leeds LS2 9JT, U.K.

Publikováno v: Inorganic chemistry [Inorg Chem] 2024 Feb 05; Vol. 63 (5), pp. 2732-2744. Date of Electronic Publication: 2024 Jan 23.

Correction: Heteroleptic iron(ii) complexes of chiral 2,6-bis(oxazolin-2-yl)-pyridine (PyBox) and 2,6-bis(thiazolin-2-yl)pyridine ligands – the interplay of two different ligands on the metal ion spin state

Autor: Shahid, N, Burrows, KE, Pask, CM, Cespedes, O, Howard, MJ, McGowan, PC, Halcrow, MA

Correction for ‘Heteroleptic iron(ii) complexes of chiral 2,6-bis(oxazolin-2-yl)-pyridine (PyBox) and 2,6-bis(thiazolin-2-yl)pyridine ligands – the interplay of two different ligands on the metal ion spin state’ by Namrah Shahid et al., Dalton

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::97d93285d3c0d53fe21834f3b186d696
https://eprints.whiterose.ac.uk/186030/1/d2dt90058k.pdf

Jahn-Teller Switching of a Redox-Active Nickel(III) Center in a Homoleptic Thiolato Metalloligand Environment.

Autor: Kouno M; Department of Chemistry, Graduate School of Science, Osaka University, Toyonaka, Osaka 560-0043, Japan.; Hyogo Prefectural Institute of Technology, Kobe, Hyogo 654-0037, Japan., Kuwamura N; Department of Chemistry, Graduate School of Science, Osaka University, Toyonaka, Osaka 560-0043, Japan.; Center for Promotion of Higher Education, Kogakuin University, Hachioji, Tokyo 192-0015, Japan., Yoshinari N; Department of Chemistry, Graduate School of Science, Osaka University, Toyonaka, Osaka 560-0043, Japan., Kojima T; Department of Chemistry, Graduate School of Science, Osaka University, Toyonaka, Osaka 560-0043, Japan., Halcrow MA; School of Chemistry, University of Leeds, Woodhouse Lane, Leeds LS2 9JT, U.K., Yamagami K; Japan Synchrotron Radiation Research Institute (JASRI), Sayo-gun, Hyogo 679-5198, Japan.; Institute for Solid State Physics, The University of Tokyo, Kashiwa, Chiba 277-8581, Japan., Sekiyama A; Division of Materials Physics, Graduate School of Engineering Science, Osaka University, Toyonaka, Osaka 560-8531, Japan., Konno T; Department of Chemistry, Graduate School of Science, Osaka University, Toyonaka, Osaka 560-0043, Japan.; Department of Chemistry, Faculty of Science, National Taiwan Normal University, Taipei 11677, Taiwan.

Publikováno v: Inorganic chemistry [Inorg Chem] 2023 Jun 19; Vol. 62 (24), pp. 9463-9470. Date of Electronic Publication: 2023 Jun 06.

Iron/2,6-di(pyrazol-1-yl)pyridine derivatives with a discotic pattern of alkyl and alkynyl substituents

Autor: Galadzhun, I, Kulmaczewski, R, Cespedes, O, Halcrow, MA

2,6-Di(4-iodopyrazol-1-yl)pyridine is converted to 2,6-di(4-{alkyn-1-yl}pyrazol-1-yl)pyridine ( L 1 R; R’ = C n H 2 n ‒3 , n = 12, 14, 16) derivatives by Sonogashira reactions. Hydrogenation of these intermediates yields the corresponding 2,6-di(

Externí odkaz: https://explore.openaire.eu/search/publication?articleId=core_ac_uk__::4c097d9d6084d7cf2616a42168b28652