53) Ray, S.; Sharma, S.; Salzner, U.; Patil, S., The Journal of Physical Chemistry C, 2017, 121, 16088-16097.
Synthesis and Characterization of Quinoidal Diketopyrrolopyrrole Derivatives with Exceptionally High Electron Affinities.

52) Dhar, J.; Salzner, U.; Patil, S., Journal of Materials Chemistry C, 2017, 5, 7404-7430.
Trends in molecular design strategies for ambient stable n-channel organic field effect transistors.

51) Aydogan Gokturk, P., U. Salzner, L. Nyulászi, B. Ulgut, C. Kocabas and S. Suzer , Electrochimica Acta, 2017, 234, 37-42.
XPS-evidence for in-situ electrochemically-generated carbene formation.


2016:

50) Mukhopadhyay, T., B. Puttaraju, S. P. Senanayak, A. Sadhanala, R. Friend, H. A. Faber, T. D. Anthopoulos, U. Salzner, A. Meyer and S. Patil , ACS Applied Materials & Interfaces, 2016, 8, 25415-25427.
Diketopyrrolopyrrole?Diketopyrrolopyrrole Oligomers for High Performance Ambipolar Organic Transistors.

2015:

49)Dhar, J., T. Mukhopadhay, N. Yaacobi-Gross, T. D. Anthopoulos, U. Salzner, S. Swaraj and S. Patil, The Journal of Physical Chemistry B, 2015, 119, 11307-11316.
Effect of Chalcogens on Electronic and Photophysical Properties of Vinylene-Based Diketopyrrolopyrrole Copolymers.

2014:

47) U. Salzner, J. Chem. Theor. Comput, 2014, 10, 4921-4937.
Effect of Donor-Acceptor Substitution on Optoelectronic Properties of Conducting Organic Polymers.

46) U. Salzner, WIREs Comput. Mol. Sci., 2014, 4, 601-622, doi: 10.1002/wcms.1194.
Electronic structure of conducting organic polymers: insights from time-dependent density functional theory .

45) J. Dhar, C. Kanimozhi, N. Yaccobi-Gross, T. D. Anthopoulos, U. Salzner, and Satish Patil, Isr. J. Chem, 2014, 54, 817-827.
Selenium in Diketopyrrolopyrrole-based Polymers: Influence on Electronic Properties and Charge Carrier Mobilities.

44) C. Kanimozhi, N. Yaacobi-Gross, E. K. Burnett, A. L. Briseno, T. D. Anthopoulos, U. Salzner and S. Patil, Phys. Chem. Chem. Phys., 2014, 16, 17253-17265.
Use of side-chain for rational design of n-type diketopyrrolopyrrole-based conjugated polymers: what did we find out?

2013:

43) U. Salzner, J. Chem. Theor. Comput, 2013, 9, 4064-4073.
Quantitatively Correct UV-vis Spectrum of Ferrocene with TDB3LYP.

2012:

42) U. Salzner, R. Baer, AIP Conference Proceedings, 2012, 1504 , 1257-1260., DOI: 10.1063/1.4772158
Density Functional Theory Orbital Energies for Predicting Ionization Energies.

2011:

41) U. Salzner, A. Aydin, J. Chem. Theor. Comput, 2011, 7, 2568-2583.
Improved Properties of pi-Conjugated Systems with Range-Separated Density Functionals.

2010:

40) U. Salzner, J. Phys. Chem. A, 2010, 114, 10997-11007.
Modeling Photoelectron Spectra of Conjugated Oligomers with Time-Dependent Density Functional Theory

39) U. Salzner, J. Phys. Chem. A, 2010, 114, 5397-5405.
Effects of Perfluorination on Thiophene and Pyrrole Oligomers.

38) R. Baer, E. Livshits, U. Salzner, Annu. Rev. Phys. Chem., 2010, 61, 85-109.
Tuned Range-Separated Hybrids in Density Functional Theory.


2009:

37) U. Salzner, R. Baer, J. Chem. Phys., 2009, 131, 231101.
Koopmans' Springs to Life.

36) S. Okur, U. Salzner, J. Phys. Chem. A, 2008, 112, 11842-11853.
Theoretical Modeling of the Doping Process in Polypyrrole by Calculating UV/vis Absorption Spectra of Neutral and Charged Oligomers

36) F. Alkan, U. Salzner, J. Phys. Chem. A, 2008, 112, 6053-6058.
Theoretical Investigation of Excited States of Oligothiophene Anions.

35) U. Salzner, J. Phys. Chem. A, 2008, 112, 5458-5466.
Investigation of Charge Carriers in Doped Thiophene Oligomers through Theoretical Modeling of their UV/Vis Spectra.

34) N. Zamoshchik, U. Salzner, M. Bendikov, J. Phys. Chem. C, 2008, 112, 8408-8418.
Nature of Charge Carriers in Long Doped Oligothiophenes. The Effect of Counterions.

33) U. Salzner, J. Chem. Theor. Comput, 2007, 3, 1143-1157.
Theoretical Investigation of Excited States of Oligothiophenes and of Their Monocations.

32) U. Salzner, J. Chem. Theor. Comput, 2007, 3, 219-231.
Theoretical Investigation of Excited States of Large Polyene Cations as Model Systems for Lightly Doped Polyacetylene.

31) U. Salzner, in: Handbook of Theoretical and Computational Nanotechnology, Eds. M. Rieth and W. Schommers, ASP, Los Angeles 2006, 8, 203-251.
Conjugated Organic Polymers: From Bulk to Molecular Wire.

30) U. Salzner, O. Karalti and S. Durdagi, J. Mol. Model., 2006, 12 , 687-701.
Does the Donor-Acceptor Concept Work for Designing Synthetic Metals? III. Theoretical Investigation of Copolymers between Quinoid Acceptors and Aromatic Donors.

29) U. Salzner, Current Organic Chemistry, 2004, 8, 569-590.
Theoretical Design of Conducting Polymers.

2003:

28) U. Salzner, J. Phys. Chem. B, 2003, 107, 1129-1134.
Ab Initio Investigation of the Electronic Structure of Poly(difluoroacetylene).

27) U. Salzner, Synth. Met, 2003, 135-136, 311-312.
Theoretical Analysis of Poly(difluoroacetylene) PDFA.

26) U. Salzner and M. E. Köse, J. Phys. Chem. B, 2002, 106, 9221-9226.
Does the Donor-Acceptor Concept Work for Designing Synthetic Metals? 2. Theoretical Investigation of Copolymers of 4-(Dicyanomethylene-4H-cyclopenta[2,1-b:3,4-b']dithiophene and 3,4-(Ethylenedioxy)-thiophene.

25) U. Salzner, J. Phys. Chem. B, 2002, 106, 9214-9220.
Does the Donor-Acceptor Concept Work for Designing Synthetic Metals? 1. Theoretical Investigation of Poly (3-cyano-3'-hydroxybithiophene).

24) U. Salzner, Synth. Met., 2001, 119, 215-216.
Investigation of the Effect of the Donor-Acceptor Concept on Band Gap, Band Width, and Conductivity

23) U. Salzner, J. Mol. Model.,2000, 6, 195-204.
Electronic Structure Analysis of A New Quinoid Conjugated Polymer

22) U. Salzner, J. B. Lagowski, R. A. Poirier and P. G. Pickup, J. Org. Chem., 1999, 64, 7419-7425.
Theoretical Analysis of Effects of p-Conjugating Substituents on Building Blocks for Conducting Polymers.

21) N. Saraçoglu, A. Menes, S. Sayan, U. Salzner and M. Balci, J. Org. Chem., 1999, 64, 6670-6676.
Pyramidalized Double Bonds Containing Endoperoxide Linkages: Photooxygenation of Dimethyl cis-3,8-Dihydroheptalene-3,8-dicarboxylate.

20) U. Salzner and T. Kiziltepe, J. Org. Chem., 1999, 64, 764-769.
Theoretical Analysis of Substituent Effects on Building Blocks of Conducting Polymers. 3,4'-Substituted Bithiophenes.

19) U. Salzner, Synth. Met.,1999, 101, 482-483.
Density Functional Theory Invesitigation of Substituent Effects on Building Blocks of Conducting Polymers.

18) U. Salzner, J. B. Lagowski, R. A. Poirier and P. G. Pickup, Synth. Met., 1998, 96, 177-189.
Comparison of Electronic Structures of Polycylopentadiene, Polypyrrole, Polyfuran, Polysilole, Polyphosphole, Polythiophene, Polyselenophene, and Polytellurophene.

17) U. Salzner, J. B. Lagowski, R. A. Poirier and P. G. Pickup, J. Phys. Chem. A, 1998, 102, 2572-2578.
Accurate Method for Obtaining Band Gaps in Conducting Polymers Using a DFT/Hybrid Approach.

16) U. Salzner, J. B. Lagowski, R. A. Poirier and P. G. Pickup, J. Comput. Chem., 1997, 18, 1943-1953.
Design of Low Band Gap Polymers Employing Density Functional Theory - Hybrid Functionals Ameliorate the Band Gap Problem.

15) U. Salzner, S. M. Bachrach and D. C. Mulhearn, J. Comput. Chem., 1997, 18, 198-210.U. Salzner, J. B. Lagowski, R. A. Poirier and P. G. Pickup, Synth. Met., 1998, 96, 177-189.
Ab Initio Investigation of the Diels-Alder Reaction between 2H-Phosphole and Phosphaethene: A Model for Phosphole Dimerization.

14) U. Salzner and S. M. Bachrach, J. Organomet. Chem., 1997, 529, 15-22.
Cycloaddition Reactions Between 2H-Phosphole and Phosphaketene. Ab initio Examination of [2+2] and [4+2] Pathways.

13) I. H. Jenkins, U. Salzner and P. G. Pickup, Chem. Mat., 1996, 8, 1444-2450.
Conducting Copolymers of Pyridine with Thiophene, N-Methylpyrrole and Selenophene.

12) U. Salzner and S. M. Bachrach, J. Org. Chem., 1996, 61, 237-242.
Cycloaddition Reactions Between Cyclopentadiene and Ketene. Ab initio Examination of [2+2] and [4+2] Pathways.

11) U. Salzner and S. M. Bachrach,J. Org. Chem., 1995, 60, 7101-7109.
1,6-Diphospha-1,5-hexadiene and the Phospha-Cope Rearrangement: An ab-Initio Investigation.

10) S. M. Bachrach and U. Salzner, J. Mol. Struct. (THEOCHEM), 1995, 337, 201-207.
Topological Electron Density Analysis of Organosulfur Compounds.

9) U. Salzner, J. Org. Chem.,1995, 60, 986-995.
Origin of the Anomeric Effect Revisited. Theoretical Conformation Analysis of 2-Hydroxypiperidine and 2-Hydroxyhexahydropyrimidine

8) U. Salzner and S. M. Bachrach, J. Am. Chem. Soc., 1994, 116, 6850-6855.
Ab Initio Studies of the Dimerization of Ketene and Phosphaketene.

7) U. Salzner and P. v. R. Schleyer, J. Org. Chem., 1994, 59, 2138-2155.
An ab initio examination of Anomeric Effects in Tetrahydropyrans, 1,3-Dioxanes, and Glucose.

6) U. Salzner and P. v. R. Schleyer, J. Am. Chem. Soc., 1993, 115, 10231-10236.
Generalized Anomeric Effects and Hyperconjugation in CH₂(OH)₂, CH₂(SH)₂ CH₂(SeH)₂, and CH₂(TeH)₂.

5) U. Salzner and P. v. R. Schleyer, Chem. Phys. Lett., 1992, 199, 267-273.
A successful ab initio study of the adiabatic electron affinity of the methyl radical

4) U. Salzner and P. v. R. Schleyer, Chem. Phys. Lett., 1992, 190, 401-406.
CH4-nXnComparison between the stabilized X = F and the destabilized X = CN series.

3) U. Salzner and P. v. R. Schleyer, Chem. Phys. Lett., 1990, 172, 461-470.
Examination of Geometries and Electronic Structures of CaF₂ and CaCl₂.

2) U. Salzner and P. v. R. Schleyer, J. Chem. Soc. Chem. Commun., 1990, 190-192.
Are there anomeric effects involving selenium?

1) U. Salzner, P. Otto and J. Ladik, J. Comput. Chem., 1990, 11, 194-204.
Numerical Solution of a Partial Differential Equation System Describing Chemical Kinetics and Diffusion in a Cell with the Aid of Compartmentalization.