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Dickson

Cordonnier M, Uy D, Dickson R M, Kew K E, Zhang Y and Oka T 2000 Selection rules for nuclear spin modifications in ion-neutral reactions involving Hg" J. Chem. Phys. 113 3181-93... [Pg.1092]

Figure C 1.5.13. Schematic diagram of an experimental set-up for imaging 3D single-molecule orientations. The excitation laser with either s- or p-polarization is reflected from the polymer/water boundary. Molecular fluorescence is imaged through an aberrating thin water layer, collected with an inverted microscope and imaged onto a CCD array. Aberrated and unaberrated emission patterns are observed for z- and xr-orientated molecules, respectively. Reprinted with pennission from Bartko and Dickson [148]. Copyright 1999 American Chemical Society. Figure C 1.5.13. Schematic diagram of an experimental set-up for imaging 3D single-molecule orientations. The excitation laser with either s- or p-polarization is reflected from the polymer/water boundary. Molecular fluorescence is imaged through an aberrating thin water layer, collected with an inverted microscope and imaged onto a CCD array. Aberrated and unaberrated emission patterns are observed for z- and xr-orientated molecules, respectively. Reprinted with pennission from Bartko and Dickson [148]. Copyright 1999 American Chemical Society.
Figure Cl.5.14. Fluorescence images of tliree different single molecules observed under the imaging conditions of figure Cl.5.13. The observed dipole emission patterns (left column) are indicative of the 3D orientation of each molecule. The right-hand column shows the calculated fit to each observed intensity pattern. Molecules 1, 2 and 3 are found to have polar angles of (0,( ))=(4.5°,-24.6°), (-5.3°,51.6°) and (85.4°,-3.9°), respectively. Reprinted with pennission from Bartko and Dickson [148]. Copyright 1999 American Chemical Society. Figure Cl.5.14. Fluorescence images of tliree different single molecules observed under the imaging conditions of figure Cl.5.13. The observed dipole emission patterns (left column) are indicative of the 3D orientation of each molecule. The right-hand column shows the calculated fit to each observed intensity pattern. Molecules 1, 2 and 3 are found to have polar angles of (0,( ))=(4.5°,-24.6°), (-5.3°,51.6°) and (85.4°,-3.9°), respectively. Reprinted with pennission from Bartko and Dickson [148]. Copyright 1999 American Chemical Society.
Figure Cl.5.15. Molecular orientational trajectories of five single molecules. Each step in tire trajectory is separated by 300 ms and is obtained from tire fit to tire dipole emission pattern such as is shown in figure Cl.5.14. The radial component is displayed as sin 0 and tire angular variable as (ji. The lighter dots around tire average orientation represent 1 standard deviation. Reprinted witli pennission from Bartko and Dickson 11481. Copyright 1999 American Chemical Society. Figure Cl.5.15. Molecular orientational trajectories of five single molecules. Each step in tire trajectory is separated by 300 ms and is obtained from tire fit to tire dipole emission pattern such as is shown in figure Cl.5.14. The radial component is displayed as sin 0 and tire angular variable as (ji. The lighter dots around tire average orientation represent 1 standard deviation. Reprinted witli pennission from Bartko and Dickson 11481. Copyright 1999 American Chemical Society.
Bartko A P and Dickson R M 1999 Three-dimensional orientations of polymer-bound single molecules J. Chem. Phys. B 103 3053-6... [Pg.2510]

Dickson R M, Cubitt A B, Tsien R Y and Moerner W E 1997 On/off blinking and switching behaviour of single molecules of green fluorescent protein Nature 388 355-8... [Pg.2511]

One convention (Dickson. 1968) for oxygen heterocycles sets the coulomb integral at z 2f) and the resonance integral at Eor the oxirane moiety,... [Pg.199]

MOBAS was written by the author (Rogers, 1983) in BASIC to illustrate matrix inversion in molecular orbital calculations. It is modeled after a program in FORTRAN n given by Dickson (Dickson, 1968). [Pg.223]

SHMO is a simple Huckel MO program in FORTRAN that functions much as MOBAS does and is also based on the Dickson program. The SHMO source code must be compiled. Compiled SHMO is in executable code (.exe). Run SHMO from the system level (do not go into BASIC) with the single command... [Pg.223]

R. S. Dickson, Homogeneous Catalysis with Compounds of Rhodium and Iridium, Reidel, Dordrecht, The Netherlands, 1985. [Pg.71]

However, because of the low melting poiats and poor hydrolytic stabiUty of polyesters from available iatermediates, Carothers shifted his attention to linear ahphatic polyamides and created nylon as the first commercial synthetic fiber. It was nearly 10 years before. R. Whinfield and J. T. Dickson were to discover the merits of poly(ethylene terephthalate) [25038-59-9] (PET) made from aromatic terephthaUc acid [100-21-0] (TA) and ethylene glycol [107-21-1] (2G). [Pg.325]

E. M. Dickson, World Hjdrogen Energy Conference, 2C-5, University of Miami, Coral Gables, Fla., 1976. [Pg.435]

E. A. Frit2ler, V. F. Yesavage, and P. F. Dickson, Proceedings, The Second Pacific Chemical Engineering Conference, American Institute of Chemical... [Pg.358]

D. P. E. Dickson and F. J. Berry, eds., Mtfssbauer Spectroscopy Cambridge University Press, New York, 1986. [Pg.326]


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