Synthesis and Structure of (π-Arene)titanium(II) Haloaluminate Complexes with Diarylmethane Ligands

2000 ◽  
Vol 65 (2) ◽  
pp. 192-202 ◽  
Author(s):  
Volkmar Kupfer ◽  
Karel Mach ◽  
Ulf Thewalt
Keyword(s):  
Crystal Structures ◽  
Ligand Exchange ◽  
Exchange Reactions ◽  
Mild Conditions ◽  
Phenyl Rings

Novel (arene)titanium(II) haloaluminate complexes (η6-arene)Ti[(μ-X)2AlX2]2 (X = Cl, Br) were obtained from (η6-benzene)Ti[(μ-X)2AlX2]2 (X = Cl, Br) complexes by ligand exchange reactions with bis(pentamethylphenyl)methane and dimesitylmethane. The [η6-1,2,3,4,5- pentamethyl-6-(2,3,4,5,6-pentamethylbenzyl)benzene]Ti[(μ-X)2AlX2]2 (X = Cl, Br) and [η6-1,3,5- trimethyl-2-(2,4,6-trimethylbenzyl)benzene]Ti[(μ-Br)2AlBr2]2 complexes containing titanium coordinated to only one of the two phenyl rings were obtained and their crystal structures were determined. (η6-Benzene)Ti[(μ-Cl)2AlCl2]2 and dimesitylmethane afforded the (η6-mesi- tylene)Ti[(μ-Cl)2AlCl2]2 complex which is isotypic with the known bromo analogue. This product shows that Friedel-Crafts scission of aryl-alkyl bonds occurs in such systems even under mild conditions.

Some aspects of the formation and structural features of low nuclearity heterometallic carboxylates

2020 ◽  
Vol 92 (7) ◽  
pp. 1093-1110 ◽  
Author(s):  
Aleksey A. Sidorov ◽  
Natalia V. Gogoleva ◽  
Evgeniya S. Bazhina ◽  
Stanislav A. Nikolaevskii ◽  
Maksim A. Shmelev ◽  
...  
Keyword(s):  
Ligand Exchange ◽  
Direct Synthesis ◽  
Molecular Complexes ◽  
Structural Features ◽  
Exchange Reactions ◽  
Metal Core ◽  
Mild Conditions ◽  
Metal Organic ◽  
Heterometallic Carboxylates ◽  
Molecular Compounds

AbstractHeterometallic carboxylate complexes are of paramount interest in pure and applied coordination chemistry. Despite that plurality of such type compounds have been published to date, synthetic aspects of their chemistry often remain in the shadow of intriguing physical properties manifesting by these species. Present review summarizes reliable data on direct synthesis of low nuclearity molecular compounds as well as coordination polymers on their base with carboxylate-bridged {M2Mg} (M = Co2+, Ni2+, Cd2+), {M2Li2} (M = Co2+, Ni2+, Zn2+, VO2+), {M2Ln2} and {M2Ln} (M = Cu2+, Zn2+, Co2+) metal cores. Structural features and stabilization factors are considered and principal outcomes are confirmed by quantum-chemical calculations. Particular attention is paid to consideration of ligand-exchange reactions that allow controllable modification of heterometallic metal core under mild conditions giving diverse molecular complexes with modified ligand environment or Metal-Organic Frameworks with permanent porosity.

Synthesis, crystal structures and ligand exchange reactions of some heptacoodinated acetylacetonate uranium (IV) complexes

1988 ◽  
Vol 345 (3) ◽  
pp. 263-274 ◽  
Author(s):  
Cécile Baudin ◽  
Pierrette Charpin ◽  
Michel Ephritikhine ◽  
Monique Lance ◽  
Martine Nierlich ◽  
...  
Keyword(s):  
Crystal Structures ◽  
Ligand Exchange ◽  
Exchange Reactions

Voltammetric Studies of Some Novel Fe(III) Complexes with Quadridentate Ligands. The Axial Ligand-Exchange Reactions in DMF and DMSO

1995 ◽  
Vol 60 (7) ◽  
pp. 1140-1157 ◽  
Author(s):  
Ljiljana S. Jovanovic ◽  
Luka J. Bjelica
Keyword(s):  
Oxidation State ◽  
Chemical Reactions ◽  
Ligand Exchange ◽  
Kinetic Data ◽  
Central Atom ◽  
Axial Ligand ◽  
Exchange Reactions ◽  
Ligand Effect ◽  
Condensation Products ◽  
Voltammetric Studies

The electrochemistry of four novel Fe(III) complexes of the type [Fe(L)Cl], involving quadridentate ligands based on the condensation products of benzoylacetone-S-methylisothiosemicarbazone with salicylaldehyde, 5-chlorosalicylaldehyde, 3,5-dichlorosalicylaldehyde or 5-nitrosalicylaldehyde, was studied in DMF and DMSO at a GC electrode. All complexes undergo a two-step one-electron reductions, usually complicated by chemical reactions. In solutions containing Cl-, the ligand-exchange reactions Cl--DMF and Cl--DMSO take place. Stability of the chloride-containing complexes was discussed in terms of the coordinated ligand effect, oxidation state of the central atom and, in particular, of the donor effect of the solvent. Some relevant kinetic data were calculated.

A first-principles study of the atomic layer deposition of ZnO on carboxyl functionalized carbon nanotubes: the role of water molecules

2021 ◽  
Vol 23 (5) ◽  
pp. 3467-3478
Author(s):  
J. I. Paez-Ornelas ◽  
H. N. Fernández-Escamilla ◽  
H. A. Borbón-Nuñez ◽  
H. Tiznado ◽  
Noboru Takeuchi ◽  
...  
Keyword(s):  
First Principles ◽  
Ligand Exchange ◽  
Functional Group ◽  
Atomic Layer ◽  
High Reactivity ◽  
Water Molecules ◽  
Exchange Reactions ◽  
Layer Deposition ◽  
The Right

Atomic description of ALD in systems that combine large surface area and high reactivity is key for selecting the right functional group to enhance the ligand-exchange reactions.

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