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      Zero-Field SMM Behavior Triggered by Magnetic Exchange Interactions and a Collinear Arrangement of Local Anisotropy Axes in a Linear Co 3 II Complex

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          Abstract

          A new linear trinuclear Co(II) 3 complex with a formula of [{Co(μ-L)} 2Co] has been prepared by self-assembly of Co(II) ions and the N 3O 3-tripodal Schiff base ligand H 3L, which is obtained from the condensation of 1,1,1-tris(aminomethyl)ethane and salicylaldehyde. Single X-ray diffraction shows that this compound is centrosymmetric with triple-phenolate bridging groups connecting neighboring Co(II) ions, leading to a paddle-wheel-like structure with a pseudo- C 3 axis lying in the Co–Co–Co direction. The Co(II) ions at both ends of the Co(II) 3 molecule exhibit distorted trigonal prismatic CoN 3O 3 geometry, whereas the Co(II) at the middle presents an elongated trigonal antiprismatic CoO 6 geometry. The combined analysis of the magnetic data and theoretical calculations reveal strong easy-axis magnetic anisotropy for both types of Co(II) ions (| D| values higher than 115 cm –1) with the local anisotropic axes lying on the pseudo- C 3 axis of the molecule. The magnetic exchange interaction between the middle and ends Co(II) ions, extracted by using either a Hamiltonian accounting for the isotropic magnetic coupling and ZFS or the Lines’ model, was found to be medium to strong and antiferromagnetic in nature, whereas the interaction between the external Co(II) ions is weak antiferromagnetic. Interestingly, the compound exhibits slow relaxation of magnetization and open hysteresis at zero field and therefore SMM behavior. The significant magnetic exchange coupling found for [{Co(μ-L)} 2Co] is mainly responsible for the quenching of QTM, which combined with the easy-axis local anisotropy of the Co II ions and the collinearity of their local anisotropy axes with the pseudo- C 3 axis favors the observation of SMM behavior at zero field.

          Abstract

          The simultaneous occurrence of considerable magnetic exchange coupling, strong easy-axis local anisotropy, and collinear arrangement of anisotropic axes in a unique linear Co 3 II complex with triple-phenolate bridging groups leads to the suppression of QTM and the observation of slow magnetic relaxation and open hysteresis under zero field.

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          Balanced basis sets of split valence, triple zeta valence and quadruple zeta valence quality for H to Rn: Design and assessment of accuracy.

          Gaussian basis sets of quadruple zeta valence quality for Rb-Rn are presented, as well as bases of split valence and triple zeta valence quality for H-Rn. The latter were obtained by (partly) modifying bases developed previously. A large set of more than 300 molecules representing (nearly) all elements-except lanthanides-in their common oxidation states was used to assess the quality of the bases all across the periodic table. Quantities investigated were atomization energies, dipole moments and structure parameters for Hartree-Fock, density functional theory and correlated methods, for which we had chosen Møller-Plesset perturbation theory as an example. Finally recommendations are given which type of basis set is used best for a certain level of theory and a desired quality of results.
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            Fully optimized contracted Gaussian basis sets for atoms Li to Kr

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              Introduction ofn-electron valence states for multireference perturbation theory

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                Author and article information

                Journal
                Inorg Chem
                Inorg Chem
                ic
                inocaj
                Inorganic Chemistry
                American Chemical Society
                0020-1669
                1520-510X
                22 November 2023
                11 December 2023
                : 62
                : 49
                : 20030-20041
                Affiliations
                []Departamento de Química Aplicada, Facultad de Química, Universidad del País Vasco (UPV/EHU) , 20018 Donostia-San Sebastián, Spain
                []Departamento de Química Inorgánica, Facultad de Ciencias, Universidad de Granada , 18071 Granada, Spain
                [§ ]Institute for Materials Research, Tohoku University , Katahira, Sendai 980-8577, Japan
                []National High Magnetic Field Laboratory, Florida State University , Tallahassee, Florida 32310, United States
                Author notes
                Author information
                https://orcid.org/0000-0002-4666-991X
                https://orcid.org/0000-0002-2286-7727
                https://orcid.org/0000-0001-6088-1936
                https://orcid.org/0000-0002-6745-9241
                Article
                10.1021/acs.inorgchem.3c02817
                10716897
                37991724
                a742b0df-1fdc-4fc4-a8c1-e5bc33ea8a01
                © 2023 The Authors. Published by American Chemical Society

                Permits the broadest form of re-use including for commercial purposes, provided that author attribution and integrity are maintained ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 13 August 2023
                : 09 November 2023
                : 03 November 2023
                Funding
                Funded by: Consejería de Economía, Conocimiento, Empresas y Universidad, Junta de Andalucía, doi 10.13039/100016970;
                Award ID: DOC_01282
                Funded by: International Collaboration Center Institute for Materials Research,Tohoku University, doi NA;
                Award ID: NA
                Funded by: Global Institute for Materials Research Tohoku, Tohoku University, doi NA;
                Award ID: NA
                Funded by: Junta de Andalucía, doi 10.13039/501100011011;
                Award ID: P20_00692
                Funded by: Junta de Andalucía, doi 10.13039/501100011011;
                Award ID: FQM-195
                Funded by: Universidad de Granada, doi 10.13039/501100006393;
                Award ID: NA
                Funded by: Ministerio de Ciencia e Innovación, doi 10.13039/501100004837;
                Award ID: RYC2021-034288-I
                Funded by: Ministerio de Ciencia e Innovación, doi 10.13039/501100004837;
                Award ID: PID2022-138090NB-C21
                Funded by: Euskal Herriko Unibertsitatea, doi 10.13039/501100003451;
                Award ID: GIU 17/13
                Funded by: European Commission, doi 10.13039/501100000780;
                Award ID: RYC2021-034288-I
                Categories
                Article
                Custom metadata
                ic3c02817
                ic3c02817

                Inorganic & Bioinorganic chemistry
                Inorganic & Bioinorganic chemistry

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