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pro vyhledávání: '"D. H. Waldeck,§ and"'
Publikováno v:
APL Materials, Vol 9, Iss 4, Pp 040902-040902-12 (2021)
We overview experiments performed on the chiral induced spin selectivity (CISS) effect using various materials and experimental configurations. Through this survey of different material systems that manifest the CISS effect, we identify several attri
Externí odkaz:
https://doaj.org/article/99514d42dba043858617de6bbef83bda
Autor:
David N. Beratan, D. H. Waldeck
Publikováno v:
Nature Chemistry. 8:992-993
Charge transfer through DNA has been well studied over recent decades from both a biological and electronics perspective. It has now been shown that charge transfer can be accelerated one hundredfold by using highly energetic 'hot holes', revealing a
Publikováno v:
The Journal of Physical Chemistry A. 106:1917-1925
Electron-transfer rates are measured for three supramolecular species, which contain an electron donor, electron acceptor, and rigid connecting bridge. Two of the species are linear and the third species is C-shaped. The latter topology produces a 10
Autor:
N. S. Park, D. H. Waldeck
Publikováno v:
Ultrafast Phenomena.
Different functional groups and their positions in the phenyl ring of stilbene and different solvents cause differences in the dipole moment, mass, volume and the surrounding environment of the solute during isomerization. These different properties
Autor:
D. H. Waldeck, D. S. Alavi
Publikováno v:
The Journal of Chemical Physics. 98:3580-3581
Publikováno v:
The Journal of Physical Chemistry B. 103:5612-5612
Publikováno v:
Journal of Physical Chemistry B; Oct2006, Vol. 110 Issue 40, p19906-19913, 8p
Publikováno v:
Journal of Physical Chemistry B; Jan2006, Vol. 110 Issue 3, p1301-1308, 8p
Autor:
D. H. WALDECK, G. R. FLEMING
Publikováno v:
Chemischer Informationsdienst. 12
Autor:
D. M. Zeglinski, D. H. Waldeck
Publikováno v:
AIP Conference Proceedings.
The rate of photoisomerization of 4,4‐dimethoxystilbene has been studied in two solvent series. These studies reveal that a separation of solvent and intramolecular effects is possible in the n‐alkanes, but not the n‐alcohols. The experimental