Mechanochemical and thermal formation of 1H-benzotriazole coordination polymers and complexes of 3d-transition metals with intriguing dielectric properties

2016 ◽  
Vol 45 (26) ◽  
pp. 10609-10619 ◽  
Author(s):  
Franziska A. Brede ◽  
Friedrich Mühlbach ◽  
Gerhard Sextl ◽  
Klaus Müller-Buschbaum
Keyword(s):  
Dielectric Properties ◽  
Transition Metal ◽  
Transition Metals ◽  
Coordination Polymers ◽  
Metal Chlorides

Liquid-assisted grinding reactions yield a series of complexes and coordination polymers from divalent transition metal chlorides and benzotriazole that have diverse dielectric properties.

Transition Metal Chlorides Are Lewis Acids toward Terminal Chloride Attached to Late Transition Metals

2014 ◽  
Vol 53 (7) ◽  
pp. 3307-3310 ◽  
Author(s):  
Alice K. Hui ◽  
Brian J. Cook ◽  
Daniel J. Mindiola ◽  
Kenneth G. Caulton
Keyword(s):  
Transition Metal ◽  
Transition Metals ◽  
Lewis Acids ◽  
Metal Chlorides ◽  
Late Transition Metals ◽  
Late Transition

Transition metal complexes of thiabendazole

1971 ◽  
Vol 24 (7) ◽  
pp. 1369 ◽  
Author(s):  
C Kowala ◽  
KS Murray ◽  
JM Swan ◽  
BO West
Keyword(s):  
Electrical Conductivity ◽  
Transition Metal ◽  
Transition Metals ◽  
Metal Complexes ◽  
Organic Solvents ◽  
Transition Metal Complexes ◽  
Metal Ion ◽  
Magnetic Moments ◽  
Anthelmintic Activity ◽  
Metal Chlorides

Complexes of thiabendazole with transition metals (Co2+, Cu2+, Fe2+, Fe3+, Mn2+, Ni2+, and Zn2+) containing one, two, or three molecules of ligand per metal ion are described. Their spectra and magnetic moments are reported. In general, the complexes are insoluble or only slightly soluble in water or most organic solvents. Only complexes of metal chlorides are sufficiently soluble in methanol to show electrical conductivity. It is suggested that most of the insoluble complexes are of polymeric character. � The anthelmintic activity of all complexes is only slightly higher than that of thiabendazole.

Die Reaktion des Monochloramins mit Übergangsmetallchloriden / The Reaction of Monochloroamine with Transition Metal Chlorides

1973 ◽  
Vol 28 (9-10) ◽  
pp. 584-589 ◽  
Author(s):  
Heinz P. Fritz ◽  
Wolfram Treptow
Keyword(s):  
Thermal Decomposition ◽  
Transition Metal ◽  
Transition Metals ◽  
Raman Spectra ◽  
Ammonium Chloride ◽  
Ir And Raman Spectra ◽  
Metal Chlorides ◽  
Ir And Raman

The reaction of H2NCl with higher chlorides of the transition metals of groups IV to VI in CCl4 solution yields ammonium chlorocomplexes and ammonium chloride. The compounds are characterized by their IR and Raman spectra; their thermal decomposition to nitrides was studied by DTA.

Intercalation of First Row Transition Metals inside Covalent-Organic Frameworks (COF): a Strategy to Fine Tune the Electronic Properties of Porous Crystalline Materials

2018 ◽  
Author(s):  
Srimanta Pakhira ◽  
Jose Mendoza-Cortes
Keyword(s):  
Transition Metal ◽  
Transition Metals ◽  
Electronic Properties ◽  
High Surface ◽  
Electronic Devices ◽  
High Surface Area ◽  
Main Role ◽  
Covalent Organic Frameworks ◽  
Porous Network ◽  
Crystalline Materials

<div>Covalent organic frameworks (COFs) have emerged as an important class of nano-porous crystalline materials with many potential applications. They are intriguing platforms for the design of porous skeletons with special functionality at the molecular level. However, despite their extraordinary properties, it is difficult to control their electronic properties, thus hindering the potential implementation in electronic devices. A new form of nanoporous material, COFs intercalated with first row transition metal is proposed to address this fundamental drawback - the lack of electronic tunability. Using first-principles calculations, we have designed 31 new COF materials <i>in-silico</i> by intercalating all of the first row transition metals (TMs) with boroxine-linked and triazine-linked COFs: COF-TM-x (where TM=Sc-Zn and x=3-5). This is a significant addition considering that only 187 experimentally COFs structures has been reported and characterized so far. We have investigated their structure and electronic properties. Specifically, we predict that COF's band gap and density of states (DOSs) can be controlled by intercalating first row transition metal atoms (TM: Sc - Zn) and fine tuned by the concentration of TMs. We also found that the $d$-subshell electron density of the TMs plays the main role in determining the electronic properties of the COFs. Thus intercalated-COFs provide a new strategy to control the electronic properties of materials within a porous network. This work opens up new avenues for the design of TM-intercalated materials with promising future applications in nanoporous electronic devices, where a high surface area coupled with fine-tuned electronic properties are desired.</div>

Bond-length distributions for ions bonded to oxygen: Metalloids and post-transition metals

2017 ◽  
Author(s):  
Olivier Charles Gagné ◽  
Frank Christopher Hawthorne
Keyword(s):  
Transition Metal ◽  
Transition Metals ◽  
Metal Ions ◽  
Bond Length ◽  
Lone Pair ◽  
Transition Metal Ions ◽  
Oxygen Lone Pair

Bond-length distributions are examined for thirty-three configurations of the metalloid ions and fifty-six configurations of the post-transition-metal ions bonded to oxygen. Lone-pair stereoactivity is discussed.

Bond-length distributions for ions bonded to oxygen: Metalloids and post-transition metals

2017 ◽  
Author(s):  
Olivier Charles Gagné ◽  
Frank Christopher Hawthorne
Keyword(s):  
Transition Metal ◽  
Transition Metals ◽  
Metal Ions ◽  
Bond Length ◽  
Lone Pair ◽  
Transition Metal Ions ◽  
Oxygen Lone Pair

Bond-length distributions are examined for thirty-three configurations of the metalloid ions and fifty-six configurations of the post-transition-metal ions bonded to oxygen. Lone-pair stereoactivity is discussed.

Electronic properties of quasi two-dimensional transition metals chalcogenides with low-dimensional magnetism

Doklady BGUIR ◽  
2020 ◽  
Vol 18 (7) ◽  
pp. 87-95
Author(s):  
M. S. Baranava ◽  
P. A. Praskurava
Keyword(s):  
Transition Metal ◽  
Transition Metals ◽  
Exchange Interaction ◽  
Electronic Properties ◽  
Metal Atom ◽  
Transition Metal Atom ◽  
Two Dimensional ◽  
Transition Metal Atoms ◽  
Ground Magnetic ◽  
Low Dimensional

The search for fundamental physical laws which lead to stable high-temperature ferromagnetism is an urgent task. In addition to the already synthesized two-dimensional materials, there remains a wide list of possible structures, the stability of which is predicted theoretically. The article suggests the results of studying the electronic properties of MAX3 (M = Cr, Fe, A = Ge, Si, X = S, Se, Te) transition metals based compounds with nanostructured magnetism. The research was carried out using quantum mechanical simulation in specialized VASP software and calculations within the Heisenberg model. The ground magnetic states of twodimensional MAX3 and the corresponding energy band structures are determined. We found that among the systems under study, CrGeTe3 is a semiconductor nanosized ferromagnet. In addition, one is a semiconductor with a bandgap of 0.35 eV. Other materials are antiferromagnetic. The magnetic moment in MAX3 is localized on the transition metal atoms: in particular, the main one on the d-orbital of the transition metal atom (and only a small part on the p-orbital of the chalcogen). For CrGeTe3, the exchange interaction integral is calculated. The mechanisms of the formation of magnetic order was established. According to the obtained exchange interaction integrals, a strong ferromagnetic order is formed in the semiconductor plane. The distribution of the projection density of electronic states indicates hybridization between the d-orbital of the transition metal atom and the p-orbital of the chalcogen. The study revealed that the exchange interaction by the mechanism of superexchange is more probabilistic.

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