R
Richard J. Saykally
Researcher at University of California, Berkeley
Publications - 459
Citations - 42709
Richard J. Saykally is an academic researcher from University of California, Berkeley. The author has contributed to research in topics: Spectroscopy & Absorption spectroscopy. The author has an hindex of 94, co-authored 457 publications receiving 40997 citations. Previous affiliations of Richard J. Saykally include University of California & Lawrence Berkeley National Laboratory.
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Importance of electronic relaxation for inter-coulombic decay in aqueous systems.
TL;DR: These guidelines indicate that this decay process should be exhibited by broad classes of biomolecules and suggest a design criterion for targeted radiooncology protocols and show that photoelectron spectroscopy cannot resolve the current hydroxide coordination controversy.
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The pure rotational spectrum and hyperfine structure of CF studied by laser magnetic resonance
TL;DR: In this paper, a detailed analysis of the Zeeman hyperfine structure of the J = 9/2→11/2 transition in the Ω = 3/2 spin component has been determined.
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Infrared laser spectroscopy of jet-cooled carbon clusters: the nu 5 band of linear C9
TL;DR: The nu 5 antisymmetric stretching vibration of 1 sigma+g C9 has been observed using direct infrared diode laser absorption spectroscopy of a pulsed supersonic cluster beam using the most sophisticated ab initio calculation considered (CCSD).
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Determination of the Dipole Moments of Molecular Ions from the Rotational Zeeman Effect by Tunable Far-Infrared Laser Spectroscopy
TL;DR: In this article, the first experimental determination of the dipole moment of a molecular ion from the rotational Zeeman effect is presented, along with an assessment of the ultimate accuracy of the technique.
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Toward a precise determination of the acceptor switching splitting in the water dimer
Heather A. Harker,Frank N. Keutsch,Claude Leforestier,Yohann Scribano,Jia-Xiang Han,Richard J. Saykally +5 more
TL;DR: In this paper, the rotational constants and tunneling splittings were combined with estimates of ground state acceptor switching (AS) for both (H2O)2 and (D2O2)2 in order to exactly predict the fingerprints of weakly allowed E 2↔ E 1 transitions and to approximately predict their absolute frequencies.