Stark Effect and Electric Dipole Moment of D2Se

1969 ◽  
Vol 50 (9) ◽  
pp. 4118-4118 ◽  
Author(s):  
A. M. Mirri ◽  
G. Corbelli ◽  
P. Forti
Keyword(s):  
Dipole Moment ◽  
Electric Dipole Moment ◽  
Electric Dipole ◽  
Stark Effect

Microwave Spectrum and Dipole Moment of Methylenecyclobutenone

1974 ◽  
Vol 29 (10) ◽  
pp. 1498-1500 ◽  
Author(s):  
W. Czieslik ◽  
L. Carpentier ◽  
D. H. Sutter
Keyword(s):  
Dipole Moment ◽  
Electric Dipole Moment ◽  
Electric Dipole ◽  
Ground State ◽  
Stark Effect ◽  
Microwave Spectrum ◽  
Least Square ◽  
Rotational Constants ◽  
Vibrational Ground State ◽  
Least Square Fit

Abstract The microwave spectrum of Methylenecyclobutenone has been investigated in the vibrational ground state in the range of 8 to 26.5 GHz. From a least square fit of 12 lines with J ≦ 4 the rotational constants have been calculated as A =5.775664±0.000009 GHz, B = 4.312314 ± 0.000007 GHz, C = 2.467814±0.000008 GHz. The inertia defect Δ = - 0.09 amuÅ2 indicates that the molecule is planar. From Stark-effect measurements the components of the molecular electric dipole moment were obtaied as |μa| = 2.04 ± 0.02 D, |μb| = 2.70±0.03 D, |μtotal| = 3.39 ± 0.05 D.

Elektrisches Dipolmoment von TlBr und TlJ

1971 ◽  
Vol 26 (11) ◽  
pp. 1809-1812 ◽  
Author(s):  
E. Tiemann
Keyword(s):  
Dipole Moment ◽  
Electric Dipole Moment ◽  
Electric Dipole ◽  
Vibrational State ◽  
Stark Effect ◽  
Dipole Moments ◽  
Electric Dipole Moments ◽  
Ground Vibrational State ◽  
Rotational Transitions

Stark-effect measurements on pure rotational transitions of TlBr and Til are described. The derived electric dipole moments of the most abundant isotopic molecules on the ground vibrational state are:205TL79Br : | μ0| = (4.493 ± 0.050) D , 205Tl127 I | μ 0| =(4.607 ± 0.070) D .The electric dipole moment of 205Tl19F | μ 0|=4.2282 (8) D was used as standard.

Elektrisches Dipolmoment und Mikrowellen- rotationsspektrum von SiS

1969 ◽  
Vol 24 (9) ◽  
pp. 1422-1423 ◽  
Author(s):  
J. Hoeft ◽  
F.J. Lovas ◽  
T. Törring
Keyword(s):  
Dipole Moment ◽  
Electric Dipole Moment ◽  
Electric Dipole ◽  
Stark Effect ◽  
Rotational Transitions

Abstract Stark effect measurements on pure rotational transitions of SiS are described. Measurements on the ground vibra-tional state of the most abundant molecule resulted in the following electric dipole moment:

Rotational Spectrum , Electric Dipole Moment, Quadrupole Coupling , and Partial r0- Structure of 3 -Cyanothiophene

1977 ◽  
Vol 32 (8) ◽  
pp. 890-896 ◽  
Author(s):  
J. Wiese ◽  
D. H. Sutter
Keyword(s):  
Dipole Moment ◽  
Electric Dipole Moment ◽  
Electric Dipole ◽  
Stark Effect ◽  
Quadrupole Coupling Constant ◽  
Abundant Species ◽  
Rotational Spectrum ◽  
Quadrupole Coupling ◽  
Centrifugal Distortion Constants ◽  
Ring Distortion

Abstract The microwave rotational spectrum of the most abundant species of 3-Cyanothiophene was investigated for the ground vibrational state. Rotational constants and centrifugal distortion constants are given. The electric dipole moment components μa and μb and the 14N-quadrupole coupling constant X + = X bb + X cc were determined from the Stark-effect splittings and hfs-splittings respectively. The experimental results are compared to CNDO/2 calculations and are discussed with reference to ring distortion.

The Microwave Spectrum of Cyanogen Iodide-15N: Hyperfine Structure and Electric Dipole Moment Investigated by Microwave Fourier Transform Spectroscopy

1988 ◽  
Vol 43 (2) ◽  
pp. 133-137 ◽  
Author(s):  
Joachim Gripp ◽  
Helmut Dreizler
Keyword(s):  
Fourier Transform ◽  
Dipole Moment ◽  
Electric Dipole Moment ◽  
Electric Dipole ◽  
Stark Effect ◽  
Rotational Transition ◽  
Microwave Spectrum ◽  
Spin Rotation ◽  
Coupling Parameters ◽  
Cyanogen Iodide

The first rotational transition of cyanogen iodide-15N (IC15N) has been investigated by microwave Fourier transform (MWFT) Stark effect spectroscopy to determine the electric dipole moment. In addition the first four rotational transitions have been measured by MWFT spectroscopy to obtain accurate parameters for the rotational, quadrupole and spin-rotation coupling parameters.

Molekülstrahl-Resonanz-Messungen von Hyperfeinstruktur, Zeeman-und Stark-Effekt an TlCl-Isotopen in verschiedenen Schwingungszuständen / Molecular Beam Resonance Measurements of Hyperfine Structure, Zeeman- and Stark-Effect of TICl-lsotopes in Different Vibrational States

1972 ◽  
Vol 27 (1) ◽  
pp. 77-91 ◽  
Author(s):  
R. Ley ◽  
W. Schauer
Keyword(s):  
Magnetic Field ◽  
Dipole Moment ◽  
Hyperfine Structure ◽  
Electric Dipole Moment ◽  
Electric Dipole ◽  
Molecular Beam ◽  
Stark Effect ◽  
Zeeman Effect ◽  
Magnetic Shielding ◽  
Vibrational States

AbstractHyperfine structure, Stark effect and Zeeman effect of the TlCl molecule have been measured with a molecular beam apparatus using electric four poles as deflecting fields and a homogeneous electric field parallel to a superimposed magnetic field in the transition region. Electric dipole transitions were induced between the hyperfine structure levels of the first rotational state J = 1 in both strong and weak external field.The following quantities could be evaluated from the spectra: the electric dipole moment µel and the magnetic rotational dipole moment µJ of the molecule, the nuclear spin-rotational interactions c1 and c2, the scalar and tensor part of the nuclear dipole-dipole interaction dS and dT, the quadrupole coupling constant e q Q of the Cl nucleus, the anisotropy of the magnetic susceptibility ξ⊥− ξ∥ , the anisotropy of the magnetic shielding of the external magnetic field at the position of both nuclei (σ⊥- σ∥)1 and (σ⊥- σ∥)2, the magnetic moment of the Cl nucleus multiplied by the scalar part of the magnetic shielding tensor µ2 · (1 - σS)2. For the most abundant isotop 205Tl35Cl the vibrational dependence of most of these quantities was measured in the vibrational states v =0, 1, 2, 3. Isotopic effects for 203Tl35Cl, 205Tl37Cl and 203Tl37Cl were investigated in the ground vibrational state. In addition the vibrational dependence of the electric dipole moment was measured for all isotopic species.It is pointed out that the usual connections between (σ⊥- σ∥)1,2 and c1,2 and between ξ⊥− ξ∥ and µJ do not hold when the excited electronic states of the molecule obey Hund’s coupling case c, which occurs most probably in TlCl.

The electric dipole moment of the state of thioformaldehyde

1981 ◽  
Vol 59 (11) ◽  
pp. 1635-1639 ◽  
Author(s):  
W. Goetz ◽  
D. C. Moule ◽  
D. A. Ramsay
Keyword(s):  
Dipole Moment ◽  
Electric Dipole Moment ◽  
Electric Dipole ◽  
Stark Effect ◽  
Large Change ◽  
The State ◽  
Large Decrease ◽  
Stark Broadening ◽  
A Value ◽  
Analogous Transition

The Stark effect on the [Formula: see text] system of H2CS has been investigated. An analysis of the Stark broadening of the lines in the pP3 branch with J″ = 3–8 yields a value of μ′ = −2.2 ± 0.3 D. The large decrease in dipole moment on excitation (μ′ = −3.85 D) is consistent with the large change in dipole moment which has been predicted for the analogous transition in H2CO.

Elektrisches dipolmoment von InCl / Electric dipole moment of incl

1972 ◽  
Vol 27 (5) ◽  
pp. 869-870 ◽  
Author(s):  
E. Tiemann ◽  
J. Hoeft ◽  
T. Törring
Keyword(s):  
Dipole Moment ◽  
Electric Field ◽  
Electric Dipole Moment ◽  
Electric Dipole ◽  
Vapour Pressure ◽  
Vibrational State ◽  
Stark Effect ◽  
Rotational Transition ◽  
Absorption Cell ◽  
Ground Vibrational State

AbstractStark-effect measurements on the rotational transition J = 1 → 2 of InCl are described. The vapour pressure in the absorption cell was chosen so that the quadrupole hyperfine structure due to the Cl-nucleus could not be resolved. Thus we neglect this coupling in the calculation of the Stark-effect. The derived electric dipole moment in the ground vibrational state is:115In35Cl : | μ0= (3.79 ± 0.10) D.The electric dipole moment of 205Tl19F : | μ0 | = 4.2282 (8) D was used for the calibration of the electric field

Electric dipole moment of formaldehyde in the first 3A2 excited state

1970 ◽  
Vol 48 (10) ◽  
pp. 1242-1253 ◽  
Author(s):  
A. D. Buckingham ◽  
D. A. Ramsay ◽  
J. Tyrrell
Keyword(s):  
Dipole Moment ◽  
Excited State ◽  
Electric Dipole Moment ◽  
Electric Dipole ◽  
Stark Effect ◽  
A Value ◽  
Parallel Polarization ◽  
And Shifts ◽  
Field Strengths

The Stark effect on the rotational lines of the 1+–0 band of the 3A2–1A1 (π* ← n) transition of formaldehyde has been studied using field strengths up to 25 kV/cm. Measurements of the Stark splittings and shifts for the Q3(3, 3), R2(3, 3), Q2(3, 3), and Q2(5, 5) lines in parallel polarization lead to a value of 1.29 ± 0.03 D for the dipole moment of formaldehyde in its 3A2-excited state. This value is significantly smaller than the value (μ′ = 1.56 ± 0.07 D) obtained by Freeman and Klemperer for the corresponding 1A2-excited state. A few measurements on lines of the 0+–0 band of the 3A2–1A1 system show that the Stark splittings and shifts are closely similar (± 3%) to those for the 1+–0 band.The spin constants for the 3A2 state have been redetermined and are:[Formula: see text]The Stark splittings show conclusively that the line assigned in earlier work as R1(3, 3) is indeed a Q2(3, 3) line in agreement with the intensity formulas of Hougen.

Sign in / Sign up

Export Citation Format

Share Document