Search results for "stibine"

showing 6 items of 6 documents

Vibrational modes of the stibine molecule

2005

International audience; In this paper, we use the algebraic approach to describe the vibrational modes of stibine molecule (of C3v molecular symmetry group) up to 21 quanta. As the stibine molecule exhibits stretch-bend resonances, we build an algebraic pyramidal coupling operator between stretching modes and bending modes adapted to this molecule. The standard deviation associated to the fit of the vibrational levels is 1.75 cm-1.

High excited levels[ PHYS.QPHY ] Physics [physics]/Quantum Physics [quant-ph]StibineAlgebraic approachVibrational modes01 natural sciencesMolecular physicsHot bandchemistry.chemical_compound[PHYS.QPHY]Physics [physics]/Quantum Physics [quant-ph]0103 physical sciencesMolecular symmetryMoleculeSbH3 moleculePhysics::Chemical PhysicsPhysical and Theoretical Chemistry010306 general physicsSpectroscopyCouplingPhysicsQuantitative Biology::Biomolecules010304 chemical physicsGroup (mathematics)Operator (physics)Atomic and Molecular Physics and OpticschemistryMolecular vibrationJournal of Molecular Spectroscopy
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CCDC 171411: Experimental Crystal Structure Determination

2002

Related Article: F.Thomas, S.Schulz, M.Nieger, K.Nattinen|2002|Chem.-Eur.J.|8|1915|doi:10.1002/1521-3765(20020415)8:8<1915::AID-CHEM1915>3.0.CO;2-Z

Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates(mu~2~-bis(Trimethylsilyl)stibine)-tricarbonyl-dimethyl-(4-(dimethylamino)pyridyl)-gallium-nickel(0)
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CCDC 207301: Experimental Crystal Structure Determination

2004

Related Article: H.Werner, N.Mahr, J.Wolf, A.Fries, M.Laubender, E.Bleuel, R.Garde, P.Lahuerta|2003|Organometallics|22|3566|doi:10.1021/om0302037

Space GroupCrystallographyCrystal Systemtrans-Chloro-(tetrachlorocyclopentadienonediazo)-bis(tri-isopropylstibine)-rhodium(i)Crystal StructureCell ParametersExperimental 3D Coordinates
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STUDY OF THE INTERNAL DYNAMICS OF NON PLANAR PYRAMIDAL MOLECULES IN VIBRATIONALY VERY EXCITED STATES.

2007

From the U (p+1) formalism, we built a Hamiltonian adapted to the stretching modes of nonplanar XY3 molecules having the C3v group of geometrical invariance. This Hamiltonian is then coupled with two possible Hamiltonians describing the bending modes of these molecular system: a) based on the U (p+1) approach, a bending Hamiltonian is developed and the interaction between the bending and the stretching modes is taking into account through adapted 2:1 resonance coupling operator defined as a Us(4) x Ub(4) enveloping algebra operator ; b) based on the standard normal modes formalism, a bending modes Hamiltonian is expanded and the 2:1 interaction is taken into account as a tensorial product o…

Spectroscopie moléculaire[ PHYS.PHYS.PHYS-ATOM-PH ] Physics [physics]/Physics [physics]/Atomic Physics [physics.atom-ph]phosphinerésonances.approche algébriquevibrationstibine[PHYS.PHYS.PHYS-ATOM-PH] Physics [physics]/Physics [physics]/Atomic Physics [physics.atom-ph]algebraic approachMolecular spectroscopyarsine
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Algebraic study of pyramidal molecules in the very excited vibrational states.

2005

In the frame of the algebraic formalism U(p+1), we developed the method to build a vibrational Hamiltonian corresponding to a set of three identical oscillators. In order to test the model, we apply it to the molecules of stibine and arsine. We introduce a supplementary intermediate group K(3) inspired by the similar formalism used in nuclear physics. This group K(3) gives additional labels for classification of the energy levels. The eigenvalues of these invariant operators distinguish the local states of the molecule. Then we study the coupling of the vibrational modes of stretching and bending for the non plane XY3 molecules. We present the construction of an algebraic operator of coupli…

Spectroscopie moléculairepyramidal moleculesunitary groupsmolécules pyramidales[ PHYS.PHYS.PHYS-ATOM-PH ] Physics [physics]/Physics [physics]/Atomic Physics [physics.atom-ph]groupes unitaires[PHYS.PHYS.PHYS-ATOM-PH] Physics [physics]/Physics [physics]/Atomic Physics [physics.atom-ph]approche algébriquevibrationstibinealgebraic approachMolecular spectroscopyarsine
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Über die wirksamkeit von lewis-basen als initiatoren der anionischen polymerisation von formaldehyd. 27. Mitt. über polyoxymethylene

1966

Die anionische Polymerisation des monomeren Formaldehydes mit LEWIS-Basen wurde bei −78°C in Ather, Aceton und Toluol untersucht. Die Basizitat der LEWIS-Basen ist ein wichtiger Faktor for ihre Initiatoraktivitat, ist jedoch nicht allein entscheidend; es spielen auch strukturelle und steren rische Faktoren eine Rolle. Primare Amine sind wahrscheinlich deshalb schlechte Initiatoren, weil sie mit Formaldehyd Methylol- und Dimethylolamine bilden. Verzweigungen aliphatischer Substituenten wirken sich um so starker retardierend aus, je naher sich die Verzweigungsstelle am Stickstoffatom befindet. Die Polymerisationsgeschwindigkeit steigt bei den meisten Aminen mit zunehmender Polaritat des Losun…

chemistry.chemical_compoundTriphenylarsineAnionic addition polymerizationchemistryPolymerizationPolymer chemistryAmine gas treatingTriphenylstibineEtherLewis acids and basesTriphenylphosphineDie Makromolekulare Chemie
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