Publications

2020

2019

2018

1 Synthesis and characterization of organic light-emitting molecules possessing 3-(4-methoxyphenyl) thieno [3, 2-b] thiophene and boron”, Cinar, M. E., Engur, E. ve Ozturk, T.,  (2018), ORGANIC COMMUNICATIONS, 11(2), 68–74. doi:10.25135/acg.oc.45.18.05.103

2 Thieno[2,3- b ]thiophene based polymers: Synthesis and optoelectronic properties.Cinar, M. E., Cankaya, S. T., Capan, A., Eroglu, M. S., & Ozturk, T. (2018).  European Polymer Journal, 104, 72–80. doi:10.1016/j.eurpolymj.2018.0

3 Recent advances on 3-hydroxyflavone derivatives: Structures and properties” B Butun, G Topcu, T Ozturk. Mini reviews in medicinal chemistry 18 (2), 98-103

4Poly (thienothiophenylborane) s and poly (dithienothiophenylborane) s for white light emitting diodes.” T Ozturk, E Tekin, O Sahin, EB Sevinis, MS Eroglu, AC Goren, ME Cinar, … US Patent 9,944,761

5Thienothiophene—boron (donor-acceptor) based materials for organic light emitting diodes.” T Ozturk, E Tekin, SP Mucur, AC Goren, G Turkoglu, ME Cinar, A Buyruk US Patent 10,000,513

6Thieno [2, 3-b] thiophene based polymers: Synthesis and optoelectronic properties.” ME Cinar, ST Cankaya, A Capan, MS Eroglu, T Ozturk European Polymer Journal 104, 72-80

7Synthesis and characterization of a bis-pyrazoline derivative as corrosion inhibitor for A283 carbon steel in 1M HCl: electrochemical, surface, DFT and MD simulation studies.” I Selatnia, A Sid, M Benahmed, T Ozturk, N Gherraf Protection of Metals and Physical Chemistry of Surfaces 54 (6), 1182-1193

2017

1 “Synthesis and Characterization of Dithienothiophene, Bithiazole and Thiophene Containing Polymer”, B. Ustamehmetoglu, I. Osken, M.E. Cinar, E. Sezer, E. Karaca, T. Ozturk, Electrochimica Acta 2017, 227, 435-446.

2  “Antioxidant and Anticholinesterase Activities of Some Dialkylamino Substituted 3-hydroxyflavone Derivatives”, B. Culhaoglua, A. Capan, M. Boga, M. Ozturk, T. Ozturk, G. Topcu, Medicinal Chemistry, 2017, 13, 1-6, DOI: 10.2174/1573406412666161104121642

 “White Light Emitting Polymers Possessing Thienothiophene and Boron Units”, O. Sahin,M. E. Cinar, E. Tekin,S. P. Mucur,S. Topal,G. Suna,M. S. Eroglu, T. Ozturk, Chemistry Select, 2017, 2, 2889-2894

4  ”New copolymers with thieno[3,2-b]thiophene or dithieno[3,2-b:2′,3′-d]thiophene units possessing electron-withdrawing 4-cyanophenyl groups: Synthesis and photophysical, electrochemical, and electroluminescent properties”, Drahomír Výprachtický, Ilknur Demirtas, Vagif Dzhabarov, Veronika Pokorná, Erdal Ertas, Turan Ozturk and Věra Cimrová, Journal of Polymer Chemistry : Part A, 2017,  DOI: 10.1002/pola.2865

5    ”Electrochemical oxidation mechanism of eugenol on graphene modified carbon paste electrode and its analytical application to pharmaceutical analysis”  Yildiz, G., Aydogmus, Z., Cinar, M.E., Senkal, F., Ozturk, T., 2017, Talanta , 173, pp. 1-8

6       ”Photoinduced Metal-Free Atom Transfer Radical Polymerization Using Highly Conjugated Thienothiophene Derivatives”,Ceren Kutahya, Andrit Allushi, Recep Isci, Johannes Kreutzer, Turan Ozturk,Gorkem Yilmaz, and Yusuf Yagci, 2017, Macromolecules, 50 (17), 6903–6910.

      ‘’Triarylborane-based materials for OLED applications’’Turkoglu, G., Cinar, M.E., Ozturk, T., 2017, Molecules ,22(9),1522

     ”Synthesis and Photophysical and Anion-Sensing Properties of Triarylborane-Substituted Cross-Conjugated and Conjugated Thienothiophenes”  Turkoglu, G., Cinar, M.E., Ozturk, T.,2017,European Journal of Organic Chemistry   2017(31), pp. 4552-4561

9     ” Antioxidant and anticholinesterase activities of some dialkylamino substituted 3-hydroxyflavone derivatives”  Culhaoglu, B., Capan, A., Boga, M., (…), Ozturk, T., Topcu, G. 2017,Medicinal Chemistry,13(3), pp. 254-259

10     ”Organoboron copolymers containing thienothiophene and selenophenothiophene analogues: Optical, electrochemical and fluoride sensing properties ”      Turkoglu, G., Cinar, M.E., Ozturk, T.,  2017, RSC Advances , 7(37), pp. 23197-23207

11    ”Fused thiophenes: An overview of the computational investigations”, Dikcal, F., Ozturk, T., Cinar, M.E., 2017,  Organic Communications, 10(2), pp. 56-71

12    ” Synthesis of some natural sulphonamide derivatives as carbonic anhydrase inhibitors”, Gokcen, T., Al, M., Topal, M., (…), Ozturk, T., Goren, A.C.,      2017,   Organic Communications, 10(1), pp. 15-23

2016

1 “Chemical RedOx Properties of a Donor-Acceptor Conjugated Microporous Dithienothiophene Benzene co-Polymer Formed via Suzuki-Miyaura Cross-coupling”, Hakan Bildirir, Ipek Osken, Johannes Schmidt, Turan Ozturk, Arne Thomas, ChemistrySelect 2016, 4, 748 –751

2 “Determination of Volatile Organic Compounds in Fourty Five Salvia Species by Thermal Desorption-GC-MS Technique”, Seda Damla Hatipoglu1, Nihal Zorlu, Tuncay Dirmenci, Ahmet C. Goren, Turan Ozturk, Gulacti Topcu, Rec. Nat. Prod. 2016, 10:6 659-700

3 “Novel organoboron compounds derived from thieno[3,2-b]-thiophene and triphenylamine units for OLED devices”, G. Turkoglu,M. E. Cinar, A. Buyruk, E. Tekin, S. P. Mucur, K. Kaya, T. Ozturk, J. Mater. Chem. C, 2016, 4, 6045 – 6053 DOI: 10.1039/c6tc01285j

4 “Copolymers Possessing Dithienothiophene and Boron for Optoelectronic Applications”, E. B. Sevinis, C. Sahin, M. E. Cinar, M. S. Eroglu, T. Ozturk, 2016, Polymer Engineering and Science, DOI 10.1002/pen

5 “Synthesis of Thioethers Using NEt3 Activated P4S10”, Gulsen Turkoglu, M. Emin Cinar, Turan Ozturk, Synthesis, 2016, DOI: 10.1055/s-0035-1561673

6 “A Class of Sulfonamides as Carbonic Anhydrase I and II Inhibitors”, T. Gokcen, I. Gulcin, T. Ozturk, A. C Ozturk, Ahmet C. Goren, J. Enz. Inhb. Med. Chem. 2016, DOI: 10.1080/14756366.2016.1198900

7 “Polymerization of Thienothiophenes and Dithienothiophenes via Click-Reaction for Electronic Applications”, A. Buyruk,M.E. Cinar,M. S. Eroglu, T. Ozturk, 2016, ChemistrySelect DOI:10.1002/slct.201600697

2015

1 “Thienothiophenes, Dithienothiophenes, and Thienoacenes: Syntheses, Oligomers, Polymers, and Properties” Mehmet Emin Cinar and Turan Ozturk, Chem. Rev., 2015, 115, 3036 – 3140

2 “Bis(vinylenedithio)tetrathiafulvalene analogues of BEDT-TTF”, E. Ertas, İ. Demirtas, T. Ozturk, Beilstein J. Org. Chem. 2015, 11, 403–415

3 “Green and effective route for the synthesis of monodispersed palladium nanoparticles using herbal tea extract (Stachys lavandulifolia) as a reductant, stablizer and capping agent; its application as a hemogeneous and reusable catalyst in the Suzuki coupling reactions in water”, H. Veisi, R. Ghorbani-Vaghei, S. Hemmati, M. Hajaliani, T. Ozturk, Appl. Organomet. Chem. 2015, 29, 26.

4 “Bulk heterojunction solar cells of three polythienothiophenes” Elif Alturk Parlak, Asli Capan, Nesrin Tore, Turan Ozturk, Organic Communications, 2015, 8, 36-42.

5 “Reversible Doping of a Dithienothiophene-Based Conjugated Microporous Polymer”, H. Bildirir, I. Osken, T. Ozturk, A. Thomas, Chem. Eur. J. 2015, 21, 9306 – 9311

6 “Syntheses and electronic properties of new type of donor-acceptor type copolymers for solar cell applications’, M. Ozel, I. Osken, T. Ozturk, Phosphorus, Sulfur, and Silicon and the Related Elements, 2015

7Sequence specific recognition of ssDNA by fluorophore 3-​hydroxyflavone” A. Capan, M. S. Bostan, E. Mozioglu, M. Akoz, A. C. Goren, M. S. Eroglu, T. Ozturk, J. Photochem. Photobiol. B, 2015153, 391-396.  |

2014

1 Electrochemical impedance spectroscopy study of poly[3,5-dithiophene-2-yldithieno[3,2-b;2’,3’-d]thiophene] P(Th2DTT)”, I. Osken, E. Sezer, E. Ertas, T. Ozturk, J. Electroanal. Chem. 2014, 726, 36–43.

2 Poly(2,6-di(thiophene-2-yl)-3,5bis(4-(thiophene-2-yl)phenyl)dithieno[3,2-b;2’,3’-d]thiophene)/Carbon Nanotube Composite for Capacitor Applications”, M. Ates, N. Eren, I. Osken, S. Baslilar, T. Ozturk, J. Appl. Polym. Sci. 2014, 131, 40061.

Electrochromic properties of 3-arylthieno[3,2-b]thiophenes” A. Capan, T. Ozturk, Synthetic Metals, 2014, 188, 100.

4 “Poly(2,6-di(thiophene-2-yl)-3,5bis(4-(thiophene-2-yl)phenyl)dithieno[3,2-b;2’,3’-d]thiophene)/Carbon Nanotube Composite for Capacitor Applications”, M. Ates, N. Eren, I. Osken, S. Baslilar, T. Ozturk, J. Appl. Polym. Sci. 2014, 131, 40061 (DOI: 10.1002/APP.40061).

5 “Electrochemical impedance spectroscopy study of poly[3,5-dithiophene-2-yldithieno[3,2-b;2’,3’-d]thiophene] P(Th2DTT)”, I. Osken, E. Sezer, E. Ertas, T. Ozturk, J. Electroanal. Chem. 2014, 726, 36–43.

“Green and effective route for the synthesis of monodispersed palladium nanoparticles using herbal tea extract (Stachys lavandulifolia) as a reductant, stablizer and capping agent; its application as a hemogeneous and reusable catalyst in the Suzuki coupling reactions in water”, H. Veisi, R. Ghorbani-Vaghei, S. Hemmati, M. Hajaliani, T. Ozturk, Appl. Organomet. Chem. 2014, in pres.

2013

1 “Controlled release of 5-aminosalicyliacid from chitosan based pH and temperature sensitive hydrogels” M. S. Bostan, M. Senol, T. Cig, I. Peker, A. C. Goren, T. Ozturk, M. S. Eroglu, International Journal of Biological Macromolecules, 2013, 52, 177-183.

2Fluorene–Dithienothiophene-S,S-dioxide Copolymers. Fine-Tuning for OLED Applications” I. Osken, A.S. Gundogan, E. Tekin, M. S. Eroglu, T. Ozturk, Macromolecules, 2013, 45, 9202.

3 “Syntheses and properties of 3,4-diaryldithieno[2,3-b;3’,2’-d]thiophenes” Sule Taskiran Cankaya, Asli Capan, Mehmet Emin Cinar, Ezgi Akin, Sebahat Topal, Turan Ozturk, Journal of Sulfur Chemistry, 2013, 34, 638–645.

4 “Synthesis and Characterization of pH and Temperature Sensitive Hydrogel for 5-Amino Salicylic Acid Delivery”, Bostan, M. S.; Senol, M.; Cig, T.; Peker, I.; Goren, A. C.; Ozturk, T.; Eroglu, M. S. Int. J. Biol. Macromol. 2013, 52, 177– 183

2012

1 “Selective syntheses of vinylenedithiathiophenes (VDTTs) and dithieno [2,3-b;20,30-d]thiophenes (DTTs); building blocks for p-conjugated systems”, I. Osken, O. Sahin, A.S. Gundogan, H. Bildirir, A. Capan, E. Ertas, M.S. Eroglu, J.D. Wallis, K. Topal, T. Ozturk, Tetrahedron, 2012, 68, 1216-1222.

2 “Synthesis and electronic properties of 4-cyanophenylvinylenedithiathiophene: An EDOT derivative”, O. Sucsoran, S. Bekiroglu, T. Ozturk, E. Ertas, Synthetic Metals, 2012, 162, 49-53.

3 “Facile syntheses of 3-hydroxyflavones”, S. Gunduz, A.C. Goren, T. Ozturk,  Organic Letters, 2012, 14(6), 1576-1579.

4 “Synthesis and electrochromic properties of 3,5-diphenyl-2,6-dithiophene-2-yldithieno[3,2-b;2’,3’-d]thiophene”, P. Dundar, I. Osken, O.Sahin, T. Ozturk, Synthetic Metals, 2012, 162, 1010-1015.

5 “Poly(3,5-dithiophene-2-yldithieno[3,2-b;2′,3′-d]thiophene-co-Ethylenedioxythiophene) / Glassy carbon Electrode Formation and Electrochemical Impedance Spectroscopy”, M. Ates, I. Osken, T. Ozturk,  Journal of The Electrochemical Society, 2012, 159(6), E115-E121.

6 “Concise Syntheses, Polymers, and Properties of 3‑Arylthieno[3,2‑b]thiophenes”, A. Capan, H. Veisi, A. C. Goren, T. Ozturk, Macromolecules, 2012.

2011

1 “Investigation of electrochromic properties of poly(3,5-bis(4-methoxyphenyl)dithieno[3,2-b;2′,3′-d]thiophene”, O. Sahin, I. Osken, T. Ozturk, Synthetic Metals, 2011, 161, 183-187.

2 “Long wavelength photoinitiated free radical polymerization using conjugated thiophene derivatives in the presence of onium salts”, S. Beyazit, B. Aydogan, I. Osken, T. Ozturk, Y. Yagci, Polymer Chemistry, 2011, 2,1185-1189.

3 “Electrochromic behavior of poly(3,5-bis(4-bromophenyl)dithieno[3,2-b;2′,3′-d]thiophene)”, I. Osken, H. Bildirir, T. Ozturk, Thin Solid Films, 2011, 519, 7707-7711.

4 “A theoretical approach to the formation mechanism of diphenyldithieno[3,2-b:20,30-d]thiophene from 1,8-diketone, 4,5-bis(benzoylmethylthio)thiophene:a DFT study”,C. Ozen, M. Yurtseven, T. Ozturk, Tetrahedron, 2011, 67, 6275-6280.

5 “Synthesis of silver/epoxy nanocomposites by visible light sensitization using highly conjugated thiophene derivatives”, Y. Yagci, O. Sahin, T. Ozturk, S. Marchi, S. Grassini, M. Sangermano, Reactive and Functional Polymers, 2011, 71, 857-862.

2010

1 ”A Berzelius Reagent, Phosphorus Decasulfide (P4S10), in Organic Syntheses”, T. Ozturk, E. Ertas, O. Mert, Chemical Review, 2010, 110, 3419-3478.

2 ”Evaluation of the electrochemical properties of 3-hydroxyflavone using voltammetric methods”, S. Guney, G. Yildiz, A. Capan, T. Ozturk, Electrochimica Acta, 2010, 55, 3295-3300.

3 “Application of N,N ‘-Diiodo-N,N ‘-1,2-ethandiylbis(p-toluene sulfonamide) as a New Reagent for Synthesis of 2-Arylbenzimidazoles and 2- Arylbenzothiazoles under Solvent-free Conditions”, H. Veisi, R. Ghorbani-Vaghei, A. Faraji, T. Ozturk, Chinese Journal of Chemistry, 2010, 28, 2249-2254.

2009

1 “Polythiophene derivatives by step-growth polymerization via photoinduced electron transfer reactions”, B.Aydogan, A.S. Gundogan, T. Ozturk, Y. Yagci, Chemical Communications, 2009, 41, 6300-6302.

2008

1  ”A Dithienothiophene Derivative as a Long-Wavelength Photosensitizer for Onium Salt Photoinitiated Cationic Polymerization”, B. Aydogan, A. S. Gundogan, T. Ozturk, Y. Yagci, Macromolecules, 2008, 41, 3468-3471.

2 ”Determination and analysis of the dispersive optical constants of the 5,5′,6,6′-tetraphenyl-2,2′-bi([1,3]dithiolo[4,5-b][1,4]dithiinylidene)-DDQ complex thin film” Y. Atalay, A. Basoglu, D. Avci, M. Arslan, T. Ozturk, E. Ertas, Physica B: Condensed Matter, 2008, 403 (12), 1983-1989.

3 ”Synthesis of highly functionalized BEDT-TTF analogues incorporating 1,4-dithiin rings from 1,8-diketones.”E. Ertas, F. B. Kaynak, S. Ozbey, I. Osken, T. Ozturk, Tetrahedron, 2008, 64, 10581-10589.

2007

1 ”Use of Lawesson Reagent in Organic Syntheses”, T. Ozturk, E. Ertas, O. Mert, Chemical Review, 2007, 107, 5210-5278.

2 ”New 3-hydroxyflavone derivatives for probing hydrophobic sites in microheterogeneous systems”, T. Ozturk, A. S. Klymchenko, A. Capan, S. Oncul, S. Cikrikci, S. Taskiran, B. Tasan, F. B. Kaynak, S. Ozbeyd, A. P. Demchenko, Tetrahedron, 2007, 63, 10290-10299.

3 ”Fluorescent dyes undergoing intramolecular proton transfer with improved sensitivity to surface charge in lipid bilayers”, G. M’Baye, A. S. Klymchenko, D. A. Yushchenko, V. V. Shvadchak, T. Ozturk, Y. Mely, G. Duportail, Photochem. Photobiol. Sci., 2007, 6, 71-76.

2006

1 ”Electrochromic Properties of Functionalized Dithieno[3,2-b;2′,3′-d]thiophene Homopolymer”, Olcay Mert, Elif Sahin, Erdal Ertas, Turan Ozturk, Engin A. Aydin, Levent Toppare, J. Electroanal. Chem., 2006, 591, 53-58.

2005

1 ”Dithienothiophenes”, T. Ozturk, E. Ertas, O. Mert, Tetrahedron, (review article), 2005, 61, 11055-11077.

2 ”Hydroxylation of PHU in High Yield”, M. S. Eroglu, B. Hazer, T. Ozturk, T. Cankara, J. Applied Polymer Science, 2005, 97, 2132-39.

3 ”3,4-Di(4-methoxyphenyl-2-oxoethylsulfanyl)thiophene”, S. Özbey, F. B. Kaynak, E. Ertas, T. Ozturk, Acta Crystallographica, 2005, 61, 393.

2004

1 “Electrochemical Behaviour of Some BEDT-TTF and TTF Derivatives”, E. Sezer, F. Turksoy, U. Tunca, T. Ozturk, Electrochemical Acta, 2004, 570, 101-105.

2 ”A Coincise Synthesis of Dithieno[3,2-b:2′,3′-d]thiophene”, E. Ertas, T. Ozturk, Tetrahedron. Lett., 2004, 45, 3405-3407.

2003

1 ”In Depth Study of the 1,8-Diketone Ring Formation Reaction; Synthesis of New TTF Derivatives”, F. Turksoy, J. D. Wallis, U. Tunca, T. Ozturk, Tetrahedron, 2003, 59, 8012.

2 “Principles of Designing the Two-band Microenvironment Sensitive Fluorescent Dyes Based on 3-Hydroxychromone”, A. S. Klymchenko, V. G. Pivovarenko, T. Ozturk, A. P. Demchenko, New J Chem., 2003, 27, 1336-1343.

2002

1 “Novel two-band ratiometric fluorescence probes with different location and orientation in phospholipid membranes”, A. S. Klymchenko, G. Duportail, T. Ozturk, V. G. Pivovarenko, Y. Mely, A. P. Demchenko, Chem. Biol., 2002, 9, 1199-1208.

2 ”Synthesis of Furanochromones: a New Step in Improvement of Fluorescence Properties”, A. S. Klymchenko, T. Ozturk, A. P. Demchenko, Tetrahedron Lett., 2002, 43, 7079.

2001

1 “A 3-hydroxychromone with Dramatically Improved Fluorescence Properties”, A. S. Klymchenko, T. Ozturk, V. G. Pivovarenko, A. P. Demchenko, Tetrahedron Lett., 2001, 42, 7967.

2 ”5,6-Diphenylthieno[2,3-d][1,3]dithiole-2-thione”, F. B. Kaynak, S. Ozbey, T. Ozturk, E. Ertas, Acta Crystallographica, 2001, C57, 1125.

3 ”5,6-Diphenyl[1,3]dithiolo[4,5-b]dithiine-2-thione”, F. Betül Kaynak, S. Özbey, T. Ozturk, E. Erta, Acta Crystallographica, 2001, C57, 926.

4 “Functionalised Organosulfur Donor Molecules: Synthesis of Racemic Hydroxymethyl-, Alkoxymethyl- and Dialkoxymethyl-bis(ethylenedithio)tetrathiafulvalenes”, N. Saygili, R. J. Brown, P. Day, R. Hoelzl, P. Kathirgamanathan, E. R. Mageean, T. Ozturk, M. Pilkington, M. M. B. Qayyum, S. S. Turner, L. Vorwerg, J. D. Wallis, Tetrahedron, 2001, 57, 5015.

5 “Synthesis and Spectroscopic Properties of Benzo/Naphtofuryl-3-hydroxychromones”, A. S. Klymchenko, T. Ozturk, V. G. Pivovarenko, A. P. Demchenko, Canadian J. Chemistry, 2001, 79, 358.

6 ”5-Benzyl-5-phenyl[1,3]dithiolo[4,5-d][1,3]dithiole-2-thione”, F.B. Kaynak, S. Ozbey, T. Ozturk, E. Ertas, Acta Crystallographica, 2001, C57, 319.

7 “Novel Organosulfur Donors Containing Hydroxy functionalities: Synthesis of bis[2,2-bis(hydroxymethyl)propane-1,3-diyldithio]tetrathiafulvalene and Related Materials” T. Ozturk, N. Saygili, S. Ozkara, M. Pilkington, C. R. Rice, D. A. Tranter, F. Turksoy, J. D. Wallis, J. Chem. Soc., Perkin Trans. 1, 2001, 407.

2000

1 ”A Concise Synthesis of 5,6-Diphenyl[1,3]dithiolo[4,5-b][1,4]dithiine-2-thione; An important Application of 1,8-Diketone Ring Closure”, E. Ertas, T. Ozturk, J. Chem. Soc., Chem. Commun. 2000, 2039.

2 ”The Synthesis of Pyrido[2,3,4-kl]acridine Unit of Some Marine Alkaloids”, T. Ozturk, A. McKillop, Canadian J. Chemistry, 2000, 78, 1158.

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