Ori Gidron Research Group
Organic Electronic Materials

25. Radical Cations of Twisted Acenes: Chiroptical Properties and Spin Delocalization

Bedi, A.; Carmieli, R.; Gidron, O.*

Chem. Commun. 2019 accepted.

24. Perfluorophenyl-Bifuran: A Stable and Fluorescent Material Exhibiting Mechanofluorochromic Behavior

Yakir, H.; L. J. W. Shimon; Gidron, O.*

Helv. Chim. Act. 2019 accepted.

    Contibution to the special issue in honor of Prof. François Diederich

23. Chiroptical Properties of Twisted Acenes: Experimental and Computational Study

Bedi, A.; Gidron, O.*

Chem. Eur. J. 2019 25, 3279.

22. Multiple Diels-Alder Transformations in Linear π-Conjugated Systems

Bedi, A.; Gidron, O.*

SYNLETT (invited SYNPACTS article) 2019 30, 119.

21. Bifuran-imide: A Stable Furan Building Unit for Organic Electronics

Mulay, S. V.; Bogoslavsky, B.; Galanti, I.; Galun, E.; Gidron, O.*

J. Mater. Chem. C 2018 6, 11951-11955.

20. Helically-Locked Tethered Twistacenes

Bedi, A.; Shimon, L. J. W.; Gidron, O.*

J. Am. Chem. Soc. 2018 140, 8086–8090.

19. Macrocyclic Oligofurans: A Computational Study

Dishi, O.; Gidron, O.*

J. Org. Chem. 2018, 83, 3119-3125.

18. Regioselective Transformation of Long π-Conjugated Backbones: From Oligofurans to Oligoarenes

Phatangare, S.; Shimon, L. J. W.; Gidron, O.*

Angew. Chem. Int. Ed. 2017, 22, 16172-16177.

17. Enantiopure Alleno-Acetylenic Helicages Containing Multiple Binding Sites

Gidron, O.; Jirasek, M.; Worle, M.; Diederich, F.*

Chem. Eur. J. 2016, 22, 16172-16177.

Before joining the Hebrew University of Jerusalem

16. Homochiral [2]Catenane and Bis[2]catenane from Alleno-Acetylenic Helicates - A Highly Selective Narcissistic Self-Sorting Process

Gidron, O.; Jirasek, M.; Trapp, N.; Ebert, M-O.; Zhang, X.; Diederich, F.*

J. Am. Chem. Soc. 2015, 137, 12502–12505.

15. Mechanistic Aspects of Aryl-Halide Oxidation Addition, Coordination Chemistry and Ring-Walking by Palladium.

Zenkina, O.V.; Gidron, O.; Shimon, L. J. W.; Iron, M. A.; van der Boom, M. E.*

Chem. Eur. J. 2015, 21, 16113–16125.

14. Conducting Polyfurans by Electropolymerization of Oligofurans

Sheberla, D.*; Patra, S.; Wijsboom, Y. H.; Sharma, S.; Sheynin, Y.; Hayoun Barak, A.; Elrazek haj Yahia, A.; Gidron O.; Bendikov M.

Chem. Sci. 2015, 6, 360-371.

13. Oligofurans and Related Compounds

Gidron, O.*

Chapter in Organic Redox Systems, Wiley-VCH, Germany, 2015.

12. Chiroptical Detection of Non-Chromophoric, Achiral Guests by Enantiopure Alleno-Acetylenic Helicages

Gidron, O.; Trapp, N.; Ebert, M-O.; Diederich, F.*

Angew. Chem. Int. Ed. 2014,53, 13614-13618.

11. Oligofurans – An Emerging Class of Conjugated Oligomers for Organic Electronics

Gidron, O.*; Bendikov, M.

Angew. Chem. Int. Ed. 2014, 53, 2346-2355.

10. Outstanding Chiroptical Properties: A Signature of Enantiomerically Pure Alleno–Acetylenic Macrocycles and Monodisperse Acyclic Oligomers.

Donckle, E.; Gidron, O.; Trapp, N.; Ebert, M-O.; Diederich, F.*

Chem. Eur. J. 2014, 20, 9558-9566.

Inside Cover.

9. Study of Bifuran Linker vs. Bithiophene Linker for Rational Design of π-Conjugated Systems. What Have We Learned?

Gidron, O.; Varsano, N.; Shimon, L. J. W.; Leitus, G.; Bendikov, M.*

Chem. Commun. 2013, 49, 6256-6258.

Front Cover Page.

8. High Charge Delocalization and Conjugation in Oligofuran Molecular Wires

Gidron, O.; Diskin-Posner, Y.; Bendikov, M.*

Chem. Eur. J. 2013, 19, 13140-13150.

7. Oligofuran-Containing Molecules for Organic Electronics

Gidron, O.; Dadvand, A.; Sun, E. W.-H; Chung, I.; Shimon, L. W. J.; Bendikov, M.; Perepichka, D. F.*

J. Mater. Chem. C. 2013, 1, 4359-4367.

6. Coordination-Based Molecular Assemblies of Oligofurans and Oligothiophenes

Hayoun Barak, A.; de Ruiter, G.; Lahav, M.; Sharma, S.; Gidron, O.; Evmenenko, G.; Dutta, P.; Bendikov M.; van der Boom M. E.*

Chem. Eur. J. 2013, 19, 8821-8831.

5. α-Oligofurans Show a Sizeable Degree of π-Conjugation as Probed by Raman Spectroscopy.

Ferrón, C. C.; Delgado, C. R. M.; Gidron, O.; Sharma, S.; Sheberla, D.; Sheynin, Y.; Bendikov, M.*; Navarrete, J. T. L.; Hernández, V.*

Chem. Commun. 2012, 48, 6732-6734.

4. Reactivity of Long Conjugated Systems: Selectivity of Diels–Alder Cycloaddition in Oligofurans

>Gidron, O.; Shimon, L. J. W.; Leitus, G.; Bendikov, M.*

Org. Lett. 2012, 14, 502-505.

3. Towards "Green" Electronic Materials. a-Oligofurans as Semiconductors.

Gidron, O.; Dadvand, A.; Sheyning, Y.; Bendikov, M.*; Perepichka, D. F.*

Chem. Commun. 2011, 46, 1976-1978.

Front Cover

1. Structure of Rubrene - Planar or Twisted? Study of Substituted Rubrenes.

Paraskar, A. S.; Reddy, A.R.; Patra, A.; Wijsboom, Y. H.; Gidron, O.; Leitus, L.; Bendikov M.*

Chem. Eur. J. 2008, 14, 10639-10647.


1. Oligo- and Polyfurans, Preparation and Uses thereof

M. Bendikov, O. Gidron, 2010 WO2011024171 (A1)