Dartar, Suay

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Name Variants
Dartar, S.
Dartar, S
Job Title
Email Address
suaydartar@iyte.edu.tr
Main Affiliation
04.01. Department of Chemistry
Status
Current Staff
Website
Scopus Author ID
Turkish CoHE Profile ID
Google Scholar ID
WoS Researcher ID

Sustainable Development Goals

NO POVERTY1
NO POVERTY
0
Research Products
ZERO HUNGER2
ZERO HUNGER
0
Research Products
GOOD HEALTH AND WELL-BEING3
GOOD HEALTH AND WELL-BEING
3
Research Products
QUALITY EDUCATION4
QUALITY EDUCATION
0
Research Products
GENDER EQUALITY5
GENDER EQUALITY
0
Research Products
CLEAN WATER AND SANITATION6
CLEAN WATER AND SANITATION
0
Research Products
AFFORDABLE AND CLEAN ENERGY7
AFFORDABLE AND CLEAN ENERGY
0
Research Products
DECENT WORK AND ECONOMIC GROWTH8
DECENT WORK AND ECONOMIC GROWTH
0
Research Products
INDUSTRY, INNOVATION AND INFRASTRUCTURE9
INDUSTRY, INNOVATION AND INFRASTRUCTURE
1
Research Products
REDUCED INEQUALITIES10
REDUCED INEQUALITIES
0
Research Products
SUSTAINABLE CITIES AND COMMUNITIES11
SUSTAINABLE CITIES AND COMMUNITIES
0
Research Products
RESPONSIBLE CONSUMPTION AND PRODUCTION12
RESPONSIBLE CONSUMPTION AND PRODUCTION
0
Research Products
CLIMATE ACTION13
CLIMATE ACTION
0
Research Products
LIFE BELOW WATER14
LIFE BELOW WATER
0
Research Products
LIFE ON LAND15
LIFE ON LAND
0
Research Products
PEACE, JUSTICE AND STRONG INSTITUTIONS16
PEACE, JUSTICE AND STRONG INSTITUTIONS
0
Research Products
PARTNERSHIPS FOR THE GOALS17
PARTNERSHIPS FOR THE GOALS
0
Research Products
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No records found in other affiliations.
Scholarly Output

10

Articles

9

Views / Downloads

38723/2853

Supervised MSc Theses

1

Supervised PhD Theses

0

WoS Citation Count

126

Scopus Citation Count

132

Patents

0

Projects

0

WoS Citations per Publication

12.60

Scopus Citations per Publication

13.20

Open Access Source

4

Supervised Theses

1

JournalCount
Chemical Communications2
Dyes and Pigments1
European Journal of Inorganic Chemistry1
Journal of Materials Chemistry B1
Organic & Biomolecular Chemistry1
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Scopus Quartile Distribution

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Scholarly Output Search Results

Now showing 1 - 10 of 10
  • Article
    Citation - WoS: 23
    Citation - Scopus: 23
    Bodipy-Vinyl Dibromides as Triplet Sensitisers for Photodynamic Therapy and Triplet-Triplet Annihilation Upconversion
    (Royal Society of Chemistry, 2021) Dartar, Suay; Emrullahoğlu, Mustafa; Karakuş, Erman; Hou, Yuqi; Zhao, Jianzhang; Emrullahoğlu, Mustafa; 04.01. Department of Chemistry; 04.04. Department of Photonics; 04. Faculty of Science; 01. Izmir Institute of Technology
    We devised a new generation of halogen-based triplet sensitisers comprising geminal dibromides at the vinyl backbone of a BODIPY fluorophore. Incorporating geminal dibromides into the pi-conjugation of BODIPY enhanced intersystem crossing due to the heavy atom effect, which in turn improved the extent of excited triplet states.
  • Article
    Citation - WoS: 4
    Citation - Scopus: 4
    A Cyclopalladated Bodipy Construct as a Fluorescent Probe for Carbon Monoxide
    (Wiley, 2022) Çevik Eren, Merve; Eren, Ahmet; Tütüncü, Büşra Buse; Tütüncü, Büşra Buse; Emrullahoğlu, Mustafa; Dartar, Suay; Emrullahoğlu, Mustafa; 04.01. Department of Chemistry; 04.04. Department of Photonics; 01. Izmir Institute of Technology; 04. Faculty of Science
    By introducing a palladium ion into the backbone of BODIPY, we devised a cyclopalladated BODIPY construct that was almost non-emissive in the absence of any analyte but became highly fluorescent upon interacting with carbon monoxide (CO) in solution and in living cells. A process of ortho-carbonylation and depalladation mediated by the specific binding of CO to palladium, promoted the release of the heavy atom from the fluorophore and consequently generated a fluorescence signal with an exceptionally high (60-fold) enhancement ratio.
  • Article
    Citation - WoS: 2
    A Reaction-Based Scenario for Fluorescence Probing of Au(iii) Ions in Human Cells and Plants [2]
    (Royal Soc Chemistry, 2023) Eren, Merve Cevik; Karakaya, Hüseyin Çağlar; Eren, Ahmet; Varlıklı, Canan; Dartar, Suay; Dartar, Suay; Kaya, Beraat Umur; Kaya, Beraat Umur; Ucuncu, Muhammed; Varlıklı, Canan; Karakaya, Hüseyin Çağlar; 04.01. Department of Chemistry; 01. Izmir Institute of Technology; 04.03. Department of Molecular Biology and Genetics; 04.04. Department of Photonics; 04. Faculty of Science
    A BODIPY-based fluorophore decorated with a gold specific reactive handle (e.g., 2-alkynylallyl alcohol) displayed a ratiometric fluorescence change in response to Au3+ ions with extraordinary selectivity over other competing metal species, including Hg2+, Cu2+, Zn(2+ )and Pd2+. By way of a gold-catalyzed intramolecular cyclisation-isomerisation reaction sequence, a BODIPY construct with an extended p-conjugation transformed into a new structure with a relatively short p-system. This unique chemical transformation was accompanied by, and resulted in, a dramatic shift in the emission and absorption wavelength, which could be monitored as distinct changes in the color of the solution's emission. Apart from its outstanding analytical performance in solution, including a quick response time (<10 s), unique specificity, a high-fold ratiometric change (62-fold), and a remarkably low detection limit (358 nM), the probe also proved useful in monitoring Au3+ ions in human cells and plants (e.g., Nicotiana benthamiana).
  • Article
    Citation - Scopus: 3
    A Reaction-Based Scenario for Fluorescence Probing of Au(iii) Ions in Human Cells and Plants
    (Royal Soc Chemistry, 2023) Eren, Merve Cevik; Emrullahoğlu, Mustafa; Dartar, Suay; Varlıklı, Canan; Kaya, Beraat Umur; Varlikli, Canan; Emrullahoglu, Mustafa; 04.01. Department of Chemistry; 01. Izmir Institute of Technology; 04.04. Department of Photonics; 04. Faculty of Science
    A BODIPY-based fluorophore decorated with a gold specific reactive handle (e.g., 2-alkynylallyl alcohol) displayed a ratiometric fluorescence change in response to Au3+ ions with extraordinary selectivity over other competing metal species, including Hg2+, Cu2+, Zn2+ and Pd2+. By way of a gold-catalyzed intramolecular cyclisation-isomerisation reaction sequence, a BODIPY construct with an extended p-conjugation transformed into a new structure with a relatively short p-system. This unique chemical transformation was accompanied by, and resulted in, a dramatic shift in the emission and absorption wavelength, which could be monitored as distinct changes in the color of the solution's emission. Apart from its outstanding analytical performance in solution, including a quick response time (<10 s), unique specificity, a high-fold ratio-metric change (62-fold), and a remarkably low detection limit (358 nM), the probe also proved useful in monitoring Au3+ ions in human cells and plants (e.g., Nicotiana benthamiana).
  • Article
    Citation - WoS: 22
    Citation - Scopus: 22
    Fluorescein Propiolate: a Propiolate- Decorated Fluorescent Probe With Remarkable Selectivity Towards Cysteine
    (Royal Society of Chemistry, 2019) Karakuş, Erman; Sayar, Melike; Kaya, Beraat Umur; Kaya, Beraat Umur; Emrullahoğlu, Mustafa; Dartar, Suay; Emrullahoğlu, Mustafa; 04.01. Department of Chemistry; 01. Izmir Institute of Technology; 04.04. Department of Photonics; 04. Faculty of Science
    A fluorescent probe decorated with an alkynyl ester unit (e.g. propiolate) displayed a selective turn-on type fluorescent response towards cysteine. Following a sequential addition-cyclisation pathway mediated by the addition of cysteine, the pre-fluorescent dye rapidly transformed into a new structure and induced a fluorescent response clearly observable with the naked eye.
  • Article
    Citation - WoS: 6
    Citation - Scopus: 7
    Development of a Water-Soluble 3-Formylbodipy Dye for Fluorogenic Sensing and Cell Imaging of Sulfur Dioxide Derivatives
    (Elsevier Ltd., 2019) Işık, Murat; Dartar, Suay; Şimşek Turan, İlke; Dartar, Suay; 04.01. Department of Chemistry; 04. Faculty of Science; 01. Izmir Institute of Technology
    A new water-soluble, highly fluorogenic 3-formylBODIPY dye that enables the sensing of SO2 derivatives in aqueous buffers and cancer cells is reported. The quaternary ammonium group appended through the mesa-position of the BODIPY dye ensures water solubility. The probe exhibits high specificity for cytosolic (bi)sulfites and fluoresces brightly in human lung adenocarcinoma cells (A549). (C) 2019 Elsevier Ltd. All rights reserved.
  • Article
    Citation - WoS: 14
    Citation - Scopus: 16
    Bodipy-Based Organic Color Conversion Layers for Wleds
    (Elsevier, 2020) Yüce, Hürriyet; Dartar, Suay; Güner, Tuğrul; Kaya, Beraat Umur; Dartar, Suay; Emrullahoğlu, Mustafa; Kaya, Beraat Umur; Yüce, Hürriyet; Emrullahoğlu, Mustafa; Demir, Mustafa Muammer; Demir, Mustafa Muammer; 03.09. Department of Materials Science and Engineering; 04.01. Department of Chemistry; 01. Izmir Institute of Technology; 04.04. Department of Photonics; 03. Faculty of Engineering; 04. Faculty of Science
    The usage of organic dyes in phosphor conversion layer of WLED is an attractive approach since they have high molar extinction coefficient and photostability. Various types of organic pigments have been employed for this purpose such as BODIPY, perylene diimide, Rhodamine B, pyrene, Nile red, etc. Among those, BODIPY-based organic dyes appear to be promising candidate for white light generation. In this work, for the first time, red and green emitting BODIPY-based organic molecules have been used as colour conversion layer. These molecules were associated with PMMA in DMF solution and the resulting solution was subjected to electrospinning. Colorful electrospun mats were embedded into PDMS matrix and their free-standing PDMS composite films were used as color conversion layers over blue LED to produce white light such that CRI of 95 and CCT of 4200 K was achieved. These values show that BODIPY-based organic molecules containing fiber composites are promising candidates to be used as color conversion layers for white light applications.
  • Master Thesis
    Desing and Synthesis of Bodipy Based Photosensitizers for Photodynamic Therapy
    (Izmir Institute of Technology, 2019) Dartar, Suay; Emrullahoğlu, Mustafa; Dartar, Suay; Emrullahoğlu, Mustafa; Emrullahoğlu, Mustafa; 04.01. Department of Chemistry; 04.04. Department of Photonics; 04. Faculty of Science; 01. Izmir Institute of Technology
    Photodynamic therapy is a promising modality for the non-invasive treatment of several cancerous and non-cancerous diseases. PDT is more preferable than other therapies due to its low damage to non-targeted tissues and its controllable characteristics. The therapy involves the activation of a photosensitizer under light illumination to generate singlet oxygen which is the cytotoxic agent employed against the cancerous tissues. Thus, there is currently a great effort to develop various photosensitizers. Among these, BODIPY based photosensitizers are distinguished due to certain characteristics, including excellent photostability, high extinction coefficients and high resistance to photobleaching. In this study, we aimed to synthesize and develop new BODIPY based photosensitizers for the use of photodynamic therapy agents. BODIPY skeleton was devised using the dibromoethylene unit from the 2,6-positions in order to enhance the π-conjugation system for red shift to longer wavelengths resulting in a deep penetration of tissue. Heavy atoms such as bromine were introduced to the BODIPY core to ensure the transition from singlet states to triplet states via intersystem crossing for the generation of singlet oxygen. Photophysical properties and spectroscopic measurements of photosensitizers were performed successfully. Finally the photodynamic activities of photosensitizers in cancerous cells were also investigated.
  • Article
    Citation - WoS: 4
    Citation - Scopus: 4
    Tailored Bodipy-Based Fluorogenic Probes for Phosgene Detection: a Comparative Evaluation of Recognition Sites
    (Royal Soc Chemistry, 2024) Dartar, Suay; Emrullahoğlu, Mustafa; Kaya, Beraat Umur; Kaya, Beraat Umur; Yayak, Yanki Oncu; Vural, Ezgi; Vural, Ezgi; Dartar, Suay; Emrullahoglu, Mustafa; 01. Izmir Institute of Technology; 04.01. Department of Chemistry; 04.04. Department of Photonics; 04. Faculty of Science
    We constructed two novel boron-dipyrromethene (BODIPY)-based fluorescent probes, BOPD and BOBA, each equipped with the phosgene specific recognition units o-phenylenediamine (OPD) and o-aminobenzylamine (OBA) at the 2-position of the BODIPY core. BOPD and BOBA represent rare examples of BODIPY-based probes that operate by modulating an intramolecular charge transfer process (ICT), as validated by computational studies. We systematically compared the analytic performance of those recognition units while focusing on selectivity, fluorescence turn-on ratios and response times. Probe BOBA, equipped with OBA as the recognition unit, demonstrated a remarkably low detection limit (i.e., 1.40 nM) and a rapid response time (<10 s) for triphosgene. By comparison, BOPD, featuring an OPD unit, showed superior selectivity towards triphosgene, with a detection limit of 93 nM and a response time of up to 30 s. A portable sensing platform was developed by loading BOPD onto test strips made of TLC plates, nonwoven materials and small-headed cotton swabs, which were assessed for their effectiveness in detecting phosgene. We additionally performed the first successful application of a fluorescent probe, namely BOPD, for monitoring the accumulation of phosgene in plants.
  • Article
    Citation - WoS: 51
    Citation - Scopus: 53
    Bodipy-Au(i): a Photosensitizer for Singlet Oxygen Generation and Photodynamic Therapy
    (American Chemical Society, 2017) Üçüncü, Muhammed; Karakuş, Erman; Dartar, Suay; Sayar, Melike; Dartar, Suay; Emrullahoğlu, Mustafa; 04.01. Department of Chemistry; 04.04. Department of Photonics; 04. Faculty of Science; 01. Izmir Institute of Technology
    Upon complexation with Au(I), a photoinactive BODIPY derivative was transformed into a highly photoactive triplet sensitizer. Along with high efficiency in singlet oxygen generation (φδ = 0.84), the new BODIPY-Au(I) skeleton showed excellent photocytotoxic activity against cancer cell lines (EC50 = 2.5 nM).