Search results for "Tridentate ligand"

Catalytic epoxidation using dioxidomolybdenum(VI) complexes with tridentate aminoalcohol phenol ligands

2019

Reaction of the tridentate aminoalcohol phenol ligands 2,4-di-tert-butyl-6-(((2 hydroxyethyl)(methyl)amino)methyl)phenol (H2L1) and 2,4-di-tert-butyl-6-(((1-hydroxybutan-2-yl)amino)methyl)phenol (H2L2) with [MoO2(acac)2] in methanol solutions resulted in the formation of [MoO2(L1)(MeOH)] (1) and [MoO2(L2)(MeOH)] (3), respectively. In contrast, the analogous reactions in acetonitrile afforded the dinuclear complexes [Mo2O2(μ-O)2(L1)2] (2) and [Mo2O2(μ-O)2(L2)2] (4). The corresponding reactions with the potentially tetradentate ligand 3-((3,5-di-tert-butyl-2-hydroxybenzyl)(methyl)amino)propane-1,2-diol (H3L3) led to the formation of the mononuclear complex [MoO2(L3)(MeOH)] (5) in methanol whi…

Magneto-Structural Correlations in μ-Halo Bridged Copper(II) Chains

1987

To design synthetic pathways to systems of desired properties is a growing challenge for inorganic chemist. Our current interest in this area is focused on copper(II) chemistry. Besides to advance in the understanding of the factors determining the conformation around copper(II) in the solid state, we intend to gain insight into the chemical and structural effects that govern exchange coupling interactions in condensed species. In this context, we have approached the synthesis and characterization of a wide set of pentacoordinated Cu(LIII)XY complexes (LIII=tridentate ligand, X=coordinating anion, Y=coordinating or non-coordinating anion) showing a great structural diversity (including mono…

Metal complexes of a picolinate-based nitronyl nitroxide free radical.

2009

A nitronyl nitroxide free radical containing an appended picolinate moiety was synthesized. The resulting tridentate ligand picNN forms neutral mononuclear metal complexes of formula [M(picNN)(2)].3H(2)O (M = Mn, Co, Ni, Zn). These compounds are isostructural and crystallize in the orthorhombic Pnna space group. The metal complexes have a C(2) symmetric structure, with the metal centers lying on the binary axis and surrounded by two equivalent picNN radicals. The magnetic properties of this family of compounds indicate the presence of very strong metal-radical exchange interactions, ranging from J(Ni-rad) = -193 cm(-1) to J(Mn-rad) = -98 cm(-1). Relatively weak (J(rad-rad) = -15 cm(-1)) thr…

(Ni2), (Ni3), and (Ni2 + Ni3): A Unique Example of Isolated and Cocrystallized Ni2 and Ni3 Complexes

2009

Structural and magnetic characterization of compound {[Ni(2)(L)(2)(OAc)(2)][Ni(3)(L)(2)(OAc)(4)]}.2CH(3)CN (3) (HL = the tridentate Schiff base ligand, 2-[(3-methylamino-propylimino)-methyl]-phenol) shows that it is a rare example of a crystal incorporating a dinuclear Ni(II) compound, [Ni(2)(L)(2)(OAc)(2)], and a trinuclear one, [Ni(3)(L)(2)(OAc)(4)]. Even more unusual is the fact that both Ni(II) complexes, [Ni(2)(L)(2)(OAc)(2)] (1) and [Ni(3)(L)(2)(OAc)(4)(H(2)O)(2)].CH(2)Cl(2).2CH(3)OH (2), have also been isolated and structurally and magnetically characterized. The structural analysis reveals that the dimeric complexes [Ni(2)(L)(2)(OAc)(2)] in cocrystal 3 and in compound 1 are almost i…

Formation of novel T-shaped NNN ligands via rare-earth metal-mediated Si-H activation.

2014

Reactions of silylamides [Ln{N(SiHMe2)2}3(thf)2] with sterically crowded terphenylamine DmpNH2 (Dmp = 2,6-Mes2C6H3 with Mes = 2,4,6-Me3C6H2) afforded via a template reaction the formation of a new tridentate ligand, and derived complexes of composition [LnN{SiMe2N(Dmp)}2] (Ln = Ce, Pr) were obtained. Usage of the even more bulky amine Ar*NH2 (Ar* = 2,6-Trip2C6H3 with Trip = 2,4,6-iPr3C6H2) yielded the free protonated ligand NH{SiMe2NH(Ar*)}2.

Studies on some antimony(III) complexes with tridentate schiff base ligands

1981

Abstract The antimony(III) complexes FSb(Sab), ClSb(Sab) and ClSb(Sat) containing dianonic, potentially tridentate Schiff-base ligands with ONO(Sab 2− ) and ONS(Sat 2− ) donor atoms have been prepared and characterized. The mass spectra of these derivatives are reported. The occurrence of chelation by the tridentate ligand is inferred from the infrared data. The antimony-121 Mossbauer parameters at 4.2 K are reported. The magnitudes and the positive sign of eQV zz suggest a consistent p-character of the antimony lone-pair orbital. Observed differencies in the isomer shift and eQV zz values are discussed on the basis of the likely distribution of electron density around antimony.

Synthesis and structural characterization of titanium complexes containing a sulfinyl-bridged bis(phenolato) ligand

1998

Abstract Titanium complexes containing the novel tridentate 2,2′-sulfinylbis(6-tert-butyl-4-methylphenoxo) ligand (sibmp) were synthesized and characterized. Treatment of titanium tetra-iso-propoxide with 2,2′-sulfinylbis(6-tert-4-methylphenol) (sibmpH2) in 1:1 molar ratio afforded red-orange, sparingly soluble di-iso-propoxo derivative [Ti(sibmp)(O-i-Pr)2]2·0.5 Et2O. The single-crystal structure analysis was performed and revealed a dimeric centrosymmetric structure with a planar Ti2O2 core. The titanium center is approximately octahedral with a SO function intramolecularly coordinated at the titanium center. Treatment of sibmpH2 with titanium tetra-iso-propoxide in 2:1 molar ratio gave y…

Carboxylate Bridge Controlled Formation of Tetra‐ and Pentanuclear Nickel(II) Complexes: Synthesis, Crystal Structure, Spectroscopy and Magnetic Prop…

2019

Push‐Pull Design of Bis(tridentate) Ruthenium(II) Polypyridine Chromophores as Deep Red Light Emitters in Light‐Emitting Electrochemical Cells

2013

Light-emitting electrochemical cells (LECs) with a simple device structure were prepared by using heteroleptic bis(tridentate) ruthenium(II) complexes [1](PF6)(2)-[3](PF6)(2) as emitters. The push-pull substitution shifts the emission energy to low energy, into the NIR region. The devices emit deep red light up to a maximum emission wavelength of 755 nm [CIE (International Commission on Illumination) coordinates: x = 0.731, y = 0.269 for [3](PF6)(2)], which, to the best of our knowledge, is the lowest emission energy for LECs containing bis(tridentate) ruthenium(II) complexes. A device structure of ITO/PEDOT:PSS/ruthenium(II) complex/Ag was used, and the thickness of the emitting layer was …

Dioxomolybdenum(VI) and -Tungsten(VI) Amino Bisphenolates as Epoxidation Catalysts

2016

Low-cost metallate salts Na2MO4·2H2O (M = molybdenum, tungsten) react with a tridentate amine bisphenol bis(2-hydroxy-3-tert-butyl-5-methylbenzyl)methylamine (H2ONOtBu) under ambient conditions in acidic methanol solutions. The reactions lead to the formation of isostructural dioxo complexes [MO2(ONOtBu)(MeOH)]·MeOH in convenient yields. Spectral data as well as X-ray analyses reveal these complexes to be isostructural. Both compounds were tested as catalysts for epoxidation of olefins using cis-cyclooctene, cyclohexene, norbornene and styrene as substrates and tert-butyl hydroperoxide and hydrogen peroxide as oxidants. The molybdenum complex catalyses selectively the oxidation of cis-cyclo…