Chemistry of organosilicon compounds. 303. The missing hexasilaprismane: synthesis, x-ray analysis and photochemical reactions

1993 ◽  
Vol 115 (13) ◽  
pp. 5853-5854 ◽  
Author(s):  
Akira Sekiguchi ◽  
Tetsuo Yatabe ◽  
Chizuko Kabuto ◽  
Hideki Sakurai
Keyword(s):  
Photochemical Reactions ◽  
Organosilicon Compounds ◽  
X Ray

X-ray spectroscopic study of the nature of the oxygen-silicon bond in organosilicon compounds

1984 ◽  
Vol 25 (2) ◽  
pp. 328-330
Author(s):  
A. T. Shuvaev ◽  
B. Yu. Khel'mer ◽  
T. L. Krasnova ◽  
L. N. Mazalov ◽  
T. A. Lyubeznova
Keyword(s):  
Spectroscopic Study ◽  
Organosilicon Compounds ◽  
X Ray

scholarly journals Reactions of Dihaloboranes with Electron-Rich 1,4-Bis(trimethylsilyl)-1,4-diaza-2,5-cyclohexadienes

Molecules ◽  
2020 ◽  
Vol 25 (12) ◽  
pp. 2875
Author(s):  
Li Ma ◽  
Xiaolin Zhang ◽  
Wenbo Ming ◽  
Shengxin Su ◽  
Xiaoyong Chang ◽  
...  
Keyword(s):  
Double Bond ◽  
Nmr Spectroscopy ◽  
Diffraction Analysis ◽  
1H Nmr Spectroscopy ◽  
Variable Temperature ◽  
Organosilicon Compounds ◽  
X Ray Diffraction ◽  
X Ray ◽  
Multinuclear Nmr Spectroscopy ◽  
Bond Character

The reactions of electron-rich organosilicon compounds 1,4-bis(trimethylsilyl)-1,4-diaza-2,5-cyclohexadiene (1), 2,3,5,6-tetramethyl-1,4-bis(trimethylsilyl)-1,4-diaza-2,5-cyclohexadiene (2), and 1,1′-bis(trimethylsilyl)-1,1′-dihydro-4,4′-bipyridine (12) with B-amino and B-aryl dihaloboranes afforded a series of novel B=N-bond-containing compounds 3–11 and 13. The B=N rotational barriers of 7 (>71.56 kJ/mol), 10 (58.79 kJ/mol), and 13 (58.65 kJ/mol) were determined by variable-temperature 1H-NMR spectroscopy, thus reflecting different degrees of B=N double bond character in the corresponding compounds. In addition, ring external olefin isomers 11 were obtained by a reaction between 2 and DurBBr2. All obtained B=N-containing products were characterized by multinuclear NMR spectroscopy. Compounds 5, 9, 10a, 11, and 13a were also characterized by single-crystal X-ray diffraction analysis.

Photochemische Reaktionen von Übergangsmetall-Organyl-Komplexen mit Olefinen, XVI [1]: Photochemisch induzierte Cycloadditionen von Diphenylacetylen an Tricarbonyl(η5-2,4-dimethyl-2,4-pentadien-1-yl)mangan / Photochemical Reactions of Transition Metal Organyl Complexes with Olefins, XVI [1]: Photochemically Induced Cycloadditions of Diphenylacetylene to Tricarbonyl(η5-2,4-dimethyl-2,4-pentadien-1-yl)manganese

1996 ◽  
Vol 51 (10) ◽  
pp. 1473-1485 ◽  
Author(s):  
Cornelius G. Kreiter ◽  
Ernst-Christian Koch ◽  
Walter Frank ◽  
Guido J. Reiß
Keyword(s):  
Mass Spectra ◽  
Photochemical Reactions ◽  
Molecular Structures ◽  
Manganese Complexes ◽  
Formation Mechanisms ◽  
X Ray Diffraction ◽  
Triclinic Space Group ◽  
Space Group ◽  
X Ray

Upon UV irradiation in THF at 208 K tricarbonyl(η5-2,4-dimethyl-2,4-pentadien-1-yl)- manganese (1) yields solvent stabilized, very reactive dicarbonyl(η5-2,4-dimethyl-2,4-pentadien-1-yl)(tetrahydrofuran)manganese (2), which reacts in situ with one or two molecules of diphenylacetylene (3) and yields four manganese complexes and 1,3-dimethyl-5,6-diphenyl-bicyclo[3.2.1]oct-2-ene-7-one (5), which were separated by HPL chromatography. In addition to tricarbonyl η5-4,6 -dimethyl-1,2-diphenyl-cyclohepta-2,4-dien-1-yl)manganese (4) formed by [5+2]cycloaddition and successive 1,4-H shift, tricarbonyl{ 1′,2′,5′-η-5-methyl-2,3 -diphenyl-5- (2′-methyl-4′,5′-diphenyl-penta-1′,4′-dien-1′,5′-diyl)cyclopent-2-en-1 -one-κ-O}manganese (6) is isolated with a ligand, formed from 2,4-dimethyl-2,4-pentadien-1-yl, two units of 3 and one carbon monoxide. The ligands of tricarbonyl{ 1-4,2′-η-4,6 -dimethyl-1,2-diphenyl-5-(E-1′,2′- diphenyl-vinylen)cyclohepta-1,3-diene}manganese (7), and tricarbonyl{η5-4,6 -dimethyl-1,2-diphenyl-7-(E-1′,2′-diphenyl-vinyl)cyclohepta-2,4-dien-1-yl}m anganese (8) are formed from 2,4-dimethyl-2,4-pentadien-1-yl and of two molecules of 3 each. The crystal and molecular structures of 5 and 6 have been determined by single crystal X-ray diffraction. 5 crystallizes in the triclinic space group P1̅ , a = 992.0(2) pm, b = 996.8(2) pm, c = 1021.0(2) pm, a = 77.67(3)°, β = 61.17(3)°, γ = 88.68(3)°. Complex 6 crystallizes also in the triclinic space group P1̅ ,a = 1023.2(2) pm, b - 1113.8(2) pm, c = 1567.9(3) pm, α = 82.88(3)°, β = 86.93(3)°, 7 = 63.53(3)°. The constitutions of 4, 7 and 8 were elucidated from the IR, NMR and mass spectra. Possible formation mechanisms for the compounds 4-8 are proposed. Complex 7 shows hindered rotations of two phenyl groups with different barriers of energy ΔG≠316 = 68.8 kJ/mol, „ΔH≠ = 67.9 ± 0.7 kJ/mol, ΔS≠ = -2 ± 2 J/mol · K and ΔG≠296 = 60.6 kJ/mol, ΔH≠ = 57.7 ± 1.0 kJ/mol, ΔS≠ = -10 ± 2 J/mol·K due to steric interactions.

Construction of the JAERI soft X-ray beamline for actinide material sciences

1998 ◽  
Vol 5 (3) ◽  
pp. 536-538 ◽  
Author(s):  
Takeshi Nakatani ◽  
Yuji Saitoh ◽  
Yuden Teraoka ◽  
Tetsuo Okane ◽  
Akinari Yokoya
Keyword(s):  
Photochemical Reactions ◽  
Resolving Power ◽  
Photoemission Spectroscopy ◽  
X Rays ◽  
Radioactive Materials ◽  
X Ray ◽  
Line Spacing ◽  
Material Sciences ◽  
Spectroscopy Studies ◽  
Under Construction

An undulator beamline for spectroscopy studies focusing on the electronic structure of actinide materials is under construction. Linearly or circularly polarized soft X-rays are provided by employing a variably polarizing undulator. Varied-line-spacing plane gratings and a sagittal-focusing system are used to monochromatize the undulator beam, whose energy ranges from 0.3 to 1.5 keV. A resolving power of 104 is expected in the whole energy region. These components are methodically operated by the SPring-8 beamline control system. There are three experimental stations in the beamline. In one of the stations the photoemission spectroscopy experiments are carried out at a radioisotope-controlled area where actinide compounds as well as unsealed radioactive materials are usable. Other experimental stations are planned in the beamline for surface photochemical reactions and biological applications.

X-ray spectroscopic investigation of chemical bonding in some organosilicon compounds

1974 ◽  
Vol 15 (3) ◽  
pp. 369-373 ◽  
Author(s):  
A. T. Shuvaev ◽  
A. P. Zemlyanov ◽  
Yu. V. Kolodyazhnyi ◽  
O. A. Osipov ◽  
V. N. Eliseev ◽  
...  
Keyword(s):  
Chemical Bonding ◽  
Spectroscopic Investigation ◽  
Organosilicon Compounds ◽  
X Ray

Direct time-resolved studies of photochemical reactions in liquids by X-ray scattering

2001 ◽  
Vol 94-95 ◽  
pp. 493-498 ◽  
Author(s):  
A. Geis ◽  
M. Bouriau ◽  
A. Plech ◽  
F. Schotte ◽  
S. Techert ◽  
...  
Keyword(s):  
Photochemical Reactions ◽  
Time Resolved ◽  
X Ray ◽  
X Ray Scattering ◽  
Ray Scattering
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