This paper presents the analysis of the spectra of SiDF(3) in its vibrational ground and v(4) = 1 states. The pure rotational spectrum of the ground state was measured up to 903 GHz (J" = 65). Rotational, quartic, and sextic centrifugal distortion constants were accurately determined. Furthermore the parameter ||h(3) || = 7.64(11) x 10(-4) Hz was derived from the observation of A(1)-A(2) splittings of six K = 3 lines. The assignment of the v(4) = 1 spectrum was performed by combining 140 pure rotational frequencies and more than 2300 rovibrational transitions. Among them, because of the strong (+/-2, -/+4) interaction, there are more than 90 A(1)-A(2) resolved split transitions between the (l = 0, k = +/-3) ground state levels and the (l = +/-2, k = -/+1) v(4) = 1 levels. Although the v(4) band is located at about 994.3 cm(-1), the energies of the other fundamental bands are at a distance of more than 140 cm(-1). The assumption of the isolated character of the state was confirmed by the small differences between the v(4) = 1 state and the ground state parameters and by the possibility of using the D and Q reduction schemes proposed by E. I. Lobodenko, O. N. Sulakshina, V. I. Perevalov, and Vl. G. Tyuterev [J. Mol. Spectrosc. 126, 159-170 (1987)]. Copyright 1999 Academic Press.
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Rev Esc Enferm USP
January 2025
Universidade Estadual de Campinas, Faculdade de Enfermagem, Campinas, SP, Brazil.
Objective: To understand the experience of children with special health needs at school.
Method: Qualitative research using Symbolic Interactionism as a theoretical framework and assumptions of Grounded Theory as a methodological framework. Data collected in a pediatric outpatient clinic of a teaching hospital in an inland city of the state of São Paulo.
Angew Chem Int Ed Engl
January 2025
TU Dortmund: Technische Universitat Dortmund, Fakultät für Chemie und Chemische Biologie, Otto-Hahn Str.6, 44227, Dortmund, GERMANY.
This study introduces a novel class of carbon-centered diradicals: a monosubstituted C-atom stabilized by a phosphine. The diradical Ph3P→C was photochemically generated from a diazophosphorus ylide precursor (Ph3PCN2) and characterized by EPR and isotope-sensitive ENDOR spectroscopy at low temperatures. Ph3P→C features an axial zero-field splitting parameter D = 0.
View Article and Find Full Text PDFInorg Chem
January 2025
Department of Chemistry, The Johns Hopkins University, Baltimore, Maryland 21218, United States.
The hydrothermal synthesis of novel materials typically relies on both knowledge of the redox activities of all cations present in the reaction solution and a small toolset of so-called mineralizers to tune the solution's overall chemical potential. Upon the use of a less conventional mineralizer species, SiO, we show the stabilization of spiroffite-type CoTeO under less forceful hydrothermal conditions than those in previous reports. When synthesized in the presence of both SiO and each respective alkali carbonate as a secondary mineralizer, silicon substitution in place of tellurium in the host structure becomes apparent, and the corresponding disorder introduced gives rise to enhanced low-temperature ferromagnetism.
View Article and Find Full Text PDFChemistry
January 2025
Jadavpur University, Chemistry, 188 Raja S. C. Mallick Road, 700032, Kolkata, INDIA.
Two π-radical complexes containing bisazo-aromatic-centered radical anion (1•-) were synthesized through in-situ electron transfer from metal-to-ligand using [IrI] and 2-(2-Pyridylazo)azobenzene (1) in inert hydrocarbon solvent. These are characterized as diradical [IrIII(1•-)2]+[2]+ and monoradical [IrIII(1•-)Cl2(PPh3)] 3. In contrast, a rare metal-mediated hydrolytic cleavage of the C(sp2)-N bond occurred in protic solvent resulting in quaternary radical complex [IrIII(1•-)(1')(PPh3)]+(4)+.
View Article and Find Full Text PDFJ Mol Model
January 2025
Department of Physics, University of Malakand, Chakdara, Dir (Lower), 18800, KP, Pakistan.
Context: The structural stability, ground state magnetic order, electronic, elastic and thermoelectric properties of NdMn in the C15, C14 and C36 polytypic phases is investigated. The magnetic phase optimization and magnetic susceptibility reveal that NdMn is antiferromagnetic (AFM) in C36 phase; and paramagnetic (PM) in C14 and C15 phases respectively. The band profiles and electrical resistivity show the metallic nature in all these polytypic phases and reveal that the C36 phase possesses smaller resistivity.
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