Results 241 to 250 of about 3,185,930 (304)
Surgical technique for secondary pectoralis major transfer after reverse total shoulder arthroplasty to treat residual internal rotation dysfunction. [PDF]
Baek CH, Kim BT, Kim JG.
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Analysis of healthy glenohumeral arthrokinematics using four-dimensional computed tomography throughout internal rotation and forward elevation. [PDF]
Paliani KK +5 more
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The subcoracoid distance is correlated with pain and internal rotation after reverse shoulder arthroplasty. [PDF]
Klosterman EL +8 more
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The Internal Rotation of the Sun
Annual Review of Astronomy and Astrophysics, 2003▪ Abstract Helioseismology has transformed our knowledge of the Sun's rotation. Earlier studies revealed the Sun's surface rotation, but now a detailed observational picture has been built up of the internal rotation of our nearest star. Unlike the predictions of stellar-evolution models, the radiative interior is found to rotate roughly uniformly ...
Jørgen Christensen-Dalsgaard +2 more
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Rotation and internal rotation in ArH3+ and ArD3+
Chemical Physics Letters, 1988Abstract We have developed a semirigid bender model Hamiltonian to calculate the rotation and internal-rotation energy levels of ArH3+ and ArD3+. We have used this Hamiltonian to fit the data reported in M. Bogey, H. Bolvin, C. Demuynck and J.L. Destombes, Phys. Rev. Letters 58 (1987) 988. From the results of the fitting we can predict other rotation
R. Escribano, P.R. Bunker
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Adiabatic approximations to internal rotation
The Journal of Chemical Physics, 2006A number of subtle and confusing issues are addressed concerning large amplitude motion (LAM) coordinates (χ) for internal molecular motions, using the methyl rotation in acetaldehyde (CH3CHO) as a model problem. If the LAM coordinate is chosen to be one of the H–C–C–O dihedral angles ρ1, ρ2, or ρ3, it lacks the required 2π∕3 periodicity, and its use ...
Wesley D, Allen +3 more
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Internal rotation in peri-phenylnaphthalenes
The Journal of Organic Chemistry, 1978A 180o rotation about a phenyl-naphthyl bond is expected to be effectively blocked for derivatives of the peridiphenylnaphthalenes, in which steric requirements force the phenyl rings to assume a face-to-face conformation. However, surprisingly low rotational energy barriers have been found.
Clough, Roger L., Roberts, John D.
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Journal of Molecular Spectroscopy, 1986
Abstract The geometrical structure of the ground state of acetone obtained by ab initio SCF energies is compared with experimental structures mainly from microwave spectroscopy. The potential function for the internal rotational motions in acetone obtained from SCF energies is compared with experimental.
James S. Crighton, Stephen Bell
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Abstract The geometrical structure of the ground state of acetone obtained by ab initio SCF energies is compared with experimental structures mainly from microwave spectroscopy. The potential function for the internal rotational motions in acetone obtained from SCF energies is compared with experimental.
James S. Crighton, Stephen Bell
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