David Yaron
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Explore the profile of David Yaron including associated specialties, affiliations and a list of published articles.
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21
Citations
122
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Recent Articles
11.
Rastede E, Tanha M, Yaron D, Watkins S, Waggoner A, Armitage B
Photochem Photobiol Sci
. 2015 Jul;
14(9):1703-12.
PMID: 26171668
The introduction of electron donor and acceptor groups at strategic locations on a fluorogenic cyanine dye allows fine-tuning of the absorption and emission spectra while preserving the ability of the...
12.
Tanha M, Chakraborty S, Gabris B, Waggoner A, Salama G, Yaron D
J Phys Chem A
. 2014 Sep;
118(42):9837-43.
PMID: 25216181
The fluorescence of the SKC-513 ((E)-N-(9-(4-(1,4,7,10,13-pentaoxa-16-azacyclooctadecan-16-yl)phenyl)-6-(butyl(3-sulfopropyl)amino)-3H-xanthen-3-ylidene)-N-(3-sulfopropyl)butan-1-aminium) dye is shown experimentally to have high sensitivity to binding of the K(+) ion. Computations are used to explore the potential origins of this...
13.
Qiu Y, Worch J, Chirdon D, Kaur A, Maurer A, Amsterdam S, et al.
Chemistry
. 2014 May;
20(25):7746-51.
PMID: 24817444
1,4-Dimercapto-2,5-diphosphinobenzene and 3,6-bis(hexyloxy)-1,4-dimercapto-2,5-diphosphinobenzene were synthesized and combined with various acid chlorides to obtain a series of benzobisthiaphospholes. Electrochemical and photophysical properties of the substituted benzobisthiaphospholes have been evaluated, and the...
14.
Barford W, Paiboonvorachat N, Yaron D
J Chem Phys
. 2011 Jun;
134(23):234101.
PMID: 21702545
We calculate the ground state and excited state second-order dispersion interactions between parallel π-conjugated polymers. The unperturbed eigenstates and energies are calculated from the Pariser-Parr-Pople model using CI-singles theory. Based...
15.
Stadler A, Renikuntla B, Yaron D, Fang A, Armitage B
Langmuir
. 2010 Dec;
27(4):1472-9.
PMID: 21174432
Double-helical DNA was used as a template for the assembly of helical cyanine dye aggregates. The aggregates consist of cofacial dimers aligned end-to-end in the minor groove of the DNA....
16.
Yaron D, Karabinos M, Lange D, Greeno J, Leinhardt G
Science
. 2010 May;
328(5978):584-5.
PMID: 20431007
No abstract available.
17.
Molecular engineering of torsional potentials in fluorogenic dyes via electronic substituent effects
Ediz V, Lee J, Armitage B, Yaron D
J Phys Chem A
. 2008 Sep;
112(40):9692-701.
PMID: 18785691
Fluorogenic dyes such as thiazole orange (TO) and malachite green have been used in live cellular imaging due to their low quantum yield in solution but large fluorescence enhancements when...
18.
Silva G, Ediz V, Yaron D, Armitage B
J Am Chem Soc
. 2007 Apr;
129(17):5710-8.
PMID: 17411048
Unsymmetrical cyanine dyes are widely used in biomolecular detection due to their fluorogenic behavior, whereby fluorescence quantum yields can be very low in fluid solution but are significantly enhanced in...
19.
Liu L, Yaron D, Sluch M, Berg M
J Phys Chem B
. 2006 Sep;
110(38):18844-52.
PMID: 16986875
The absorption spectra of phenyleneethynylene oligomers show an unusual change in shape with oligomer length. The unusual aspects of the spectra arise from rotation of the phenylene rings about the...
20.
Janesko B, Yaron D
J Chem Phys
. 2004 Sep;
121(12):5635-45.
PMID: 15366987
Ab initio electronic structure methods give accurate results for small systems, but do not scale well to large systems. Chemical insight tells us that molecular functional groups will behave approximately...