scholarly journals Photoreductive elimination of chlorobenzene from a bimetallic Ge/Pt complex

2021 ◽  
Author(s):  
Mohammadjavad Karimi ◽  
François Gabbaï
Keyword(s):  
Pt Complex

scholarly journals Innenrücktitelbild: Multinuclear Ag Clusters Sandwiched by Pt Complex Units: Fluxional Behavior and Chiral‐at‐Cluster Photoluminescence (Angew. Chem. 19/2021)

2021 ◽  
Vol 133 (19) ◽  
pp. 11095-11095
Author(s):  
Shinnosuke Horiuchi ◽  
Sangjoon Moon ◽  
Akitaka Ito ◽  
Jacopo Tessarolo ◽  
Eri Sakuda ◽  
...  
Keyword(s):  
Pt Complex ◽  
Ag Clusters

Oxamide Oxime Complexes: The Structure of the Complex Bis ( oxamide - oximato )nickel( II) - Hydrogen Chloride - Water, and the Characterization of the Analogous Platinum(II) Complex

1982 ◽  
Vol 37 (6) ◽  
pp. 702-706 ◽  
Author(s):  
Helmut Entires
Keyword(s):  
Hydrogen Chloride ◽  
Structure Determination ◽  
Columnar Structure ◽  
Orthorhombic Symmetry ◽  
Complete Structure ◽  
Complex Molecules ◽  
Planar Complex ◽  
Pt Complex ◽  
Chloride Water

Abstract[Ni(C2H5N4O2)2] · HCl · H2O, C4H10N8NiO4 · HCl · H2O, forms triclinic crystals, Mr = 347.36, P1̄, a = 7.219(2), b = 7.316(1), c = 11.797(3) Å, α = 73.89(2), β = 86.37(2), γ = 85.71(2)°, V = 596 Å3 , Z = 2, dc = 1.93 Mgm-3 ; final Rw = 0.028 for 1957 reflections. The planar complex molecules form equidistant stacks along b, with the molecular planes inclined at ~29° to the stacking axis. Molecules of adjacent stacks are linked along a by an intermolecular H bridge coexistins with the usual intramolecular H bridges. The analogous Pt complex, C4H10N8O4Pt · HCl · H2O, Mr = 483.74, a = 6.480(4), b = 16.115(5), c = 12.194(9) Å, β = 101.27(4)°, V = 1249 Å3 , Z = 4, dc = 2.57 Mgm-3 , P21/a, crystallizes in a columnar structure with a Pt-Pt separation of ~a/2 ≈ 3.24 Å. Due to twinning, faking orthorhombic symmetry, a complete structure determination was not possible.

A 0.27V 30MHz 17.7nJ/transform 1024-pt complex FFT core with super-pipelining

2011 ◽  
Author(s):  
Mingoo Seok ◽  
Dongsuk Jeon ◽  
Chaitali Chakrabarti ◽  
David Blaauw ◽  
Dennis Sylvester
Keyword(s):  
Pt Complex

Isolation and characterization of a tetranuclear Pt–Fe⋯Fe–Pt intermediate en route to the trinuclear Pt–Fe–Pt cluster

2017 ◽  
Vol 46 (40) ◽  
pp. 14012-14020
Author(s):  
Kazuhiro Uemura ◽  
Masahiro Taoka
Keyword(s):  
Single Crystal ◽  
Intermediate Compound ◽  
Mononuclear Complex ◽  
Synthetic Process ◽  
X Ray ◽  
Pt Complex ◽  
Isolation And Characterization ◽  
Physical Measurements ◽  
Pt Cluster

An intermediate compound of a tetranuclear Pt–Fe⋯Fe–Pt complex in the synthetic process to form a trinuclear Pt–Fe–Pt complex by mixing the “amidate-hanging” Pt mononuclear complex and iron sources was successfully isolated and characterized by single-crystal X-ray analysis and several physical measurements.

scholarly journals Structure of the human heterotetrameric cis-prenyltransferase complex

2020 ◽  
Author(s):  
Michal Lisnyansky Bar-El ◽  
Pavla Vankova ◽  
Petr Man ◽  
Yoni Haitin ◽  
Moshe Giladi
Keyword(s):  
Crystal Structure ◽  
Active Site ◽  
Substrate Binding ◽  
Synthesis Mechanism ◽  
Allosteric Communication ◽  
Pt Complex ◽  
C Terminus ◽  
Length Determination ◽  
Enzymatic Complex

AbstractThe human cis-prenyltransferase (hcis-PT) is an enzymatic complex essential for protein N-glycosylation. Synthesizing the precursor of the glycosyl carrier dolichol-phosphate, we reveal here that hcis-PT exhibits a novel heterotetrameric assembly in solution, composed of two catalytic dehydrodolichyl diphosphate synthase (DHDDS) and two inactive Nogo-B receptor (NgBR) subunits. The 2.3 Å crystal structure of the complex exposes a dimer-of-heterodimers arrangement, with DHDDS C-termini serving as homotypic assembly domains. Furthermore, the structure elucidates the molecular details associated with substrate binding, catalysis, and product length determination. Importantly, the distal C-terminus of NgBR transverses across the heterodimeric interface, directly participating in substrate binding and underlying the allosteric communication between the subunits. Finally, mapping disease-associated hcis-PT mutations involved in blindness, neurological and glycosylation disorders onto the structure reveals their clustering around the active site. Together, our structure of the hcis-PT complex unveils the dolichol synthesis mechanism and its perturbation in disease.

scholarly journals Butterfly Deformation Modes in a Photoexcited Pyrazolate-Bridged Pt Complex Measured by Time-Resolved X-Ray Scattering in Solution

2016 ◽  
Vol 120 (38) ◽  
pp. 7475-7483 ◽  
Author(s):  
Kristoffer Haldrup ◽  
Asmus O. Dohn ◽  
Megan L. Shelby ◽  
Michael W. Mara ◽  
Andrew B. Stickrath ◽  
...  
Keyword(s):  
Time Resolved ◽  
X Ray ◽  
Pt Complex ◽  
X Ray Scattering ◽  
Deformation Modes ◽  
Ray Scattering

scholarly journals The effect of the morpholinium ionic liquid anion on the catalytic activity of Rh (or Pt) complex–ionic liquid systems in hydrosilylation processes

RSC Advances ◽  
2018 ◽  
Vol 8 (47) ◽  
pp. 26922-26927 ◽  
Author(s):  
Magdalena Jankowska-Wajda ◽  
Izabela Dąbek ◽  
Ryszard Fiedorow ◽  
Hieronim Maciejewski
Keyword(s):  
Ionic Liquid ◽  
Catalytic Activity ◽  
Ionic Liquids ◽  
Platinum Complexes ◽  
Pt Complex ◽  
Liquid Systems

Rhodium and platinum complexes were immobilized in morpholinium ionic liquids, the effect of which on the catalytic activity was determined.

scholarly journals Metal Complexes of π-Expanded Ligand (7): Syntheses, Structures and Properties of Pt(II) Complexes Containing the Isomeric 1- and 2-Alkyliminomethyl Pyrene Ligands

Crystals ◽  
2020 ◽  
Vol 10 (6) ◽  
pp. 476 ◽  
Author(s):  
Xuan-Dien Luong ◽  
Xuan-Truong Nguyen
Keyword(s):  
Molecular Structure ◽  
Planar Geometry ◽  
X Ray Diffraction ◽  
X Ray ◽  
Pt Complex ◽  
Physico Chemical ◽  
Clear Explanation ◽  
Square Planar ◽  
Structures And Properties ◽  
The Relationship

A [O,N] bidentate π-expanded ligand system, (E)-1-(n-octylimino)methylpyren-2-ol (2), was newly synthesized via a six-step synthesis from pyrene. The ligand 2 reacts with [PtCl2(PhCN)2] in chlorobenzene and the presence of a base at reflux for 2 h under the formation of (2(Pt)) complex with a yield of 70%. The molecular structure of (2(Pt)), studied by common spectroscopic methods and X-ray diffraction, shows a square planar geometry with a trans-configuration of the ligands. The molecular structure, absorption spectra, electrochemical properties, and phosphorescence characteristics of the (2(Pt)) complex are discussed, emphasizing the comparison with those of the previously reported Pt complex (1(Pt)) containing the isomeric ligands of 2, (E)-2-(n-octylimino)methylpyren-1-ol. The DFT calculations of the two Pt complexes are carried out and exhibit a clear explanation of the relationship between their physico-chemical characteristics.

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