Ertan, Salih

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Profile URL
https://hdl.handle.net/20.500.14411/6700
Name Variants
Ertan, Salih
Ertan,Salih
S., Ertan
Ertan,S.
E.,Salih
Salih Ertan
Salih, Ertan
E., Salih
S.,Ertan
Job Title
Doktor Öğretim Üyesi
Email Address
salih.ertan@tilim.edu.tr
Main Affiliation
Chemical Engineering
Status
Website
ORCID ID
0000-0001-8852-1879
Scopus Author ID
55240269100
Turkish CoHE Profile ID
Google Scholar ID
OnUYChYAAAAJ
WoS Researcher ID
M-6370-2013

Sustainable Development Goals

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

9

Citations

162

h-index

7

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Documents

10

Citations

169

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Scholarly Output

10

Articles

9

Views / Downloads

68/142

Supervised MSc Theses

1

Supervised PhD Theses

0

WoS Citation Count

121

Scopus Citation Count

124

Patents

0

Projects

0

WoS Citations per Publication

12.10

Scopus Citations per Publication

12.40

Open Access Source

0

Supervised Theses

1

JournalCount
Dyes and Pigments3
Electrochimica Acta2
Journal of Polymer Science Part A: Polymer Chemistry1
Macromolecules1
Materials Today Communications1
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2018 - 20192
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Author: Onal, Ahmet M.

Scholarly Output Search Results

Now showing 1 - 2 of 2
  • Thumbnail Image
    Article
    Citation - WoS: 11
    Citation - Scopus: 11
    Electrochemical and Optical Properties of Substituted Phthalimide Based Monomers and Electrochemical Polymerization of 3,4-Ethylenedioxythiophene Oligomeric Silsesquioxane (poss) Analogue
    (Elsevier Sci Ltd, 2019) Cakal, Deniz; Ertan, Salih; Cihaner, Atilla; Onal, Ahmet M.
    A new series of donor-acceptor-donor type trimeric monomers bearing substituted phthalimide units as acceptor units and thiophene and 3,4-ethylenedioxythiophene (EDOT) as donor units was synthesized and characterized. The strength of acceptor units and intramolecular charge transfer between donor and acceptor units were investigated by using electrochemical and optical methods. The main advantage of phthalimide unit over other acceptor units is the ease of its functionalizability. Thus, utilizing this property, a phthalimide derivative (E2P-POSS) bearing polyhedral oligomeric silsesquioxane (POSS) cage was introduced successfully with EDOT and polymerized electrochemically. The corresponding electroactive polymer, PE2P-POSS, has a band gap of 1.72 eV and is an electrochromic polymer: gray when neutralized and eggplant purple when oxidized.
  • Thumbnail Image
    Article
    Citation - WoS: 24
    Citation - Scopus: 23
    Synthesis and Electrochemical Polymerization of D-A Type Monomers With Thieno [3,4-c] Pyrrole-4,6 Acceptor Unit
    (Elsevier Sci Ltd, 2018) Cakal, Deniz; Ertan, Salih; Cihaner, Atilla; Onal, Ahmet M.
    In this study, three new donor-acceptor-donor type monomers bearing 1,3-dibromo-5-(2-ethylhexyl)-4H-thieno [3,4-c]pyrrole- 4,6(5H)-dione (A) as an acceptor unit and thiophene, 3,4-ethylenedioxythiophene (EDOT) and 3,3-didecy1-3,4-dihydro-2H-thieno[3,4-b][1,4]dioxepine (didecyl-ProDOT) as donor units were synthesized via Stille cross-coupling reaction and their electrochemical polymerization by repetitive cycling was reported. The electrochemical and optical properties of the monomers ((5-(2-ethyl-liexyl)-1,3-di(thienyl-2-yl)-4H-thienolr-3,4-cl pyrrole-4,6(5H)-dione (TAT), 1,3-bis(2,3-dihydrothieno[3,4-1)] (1,4]dioicin-5-yl)-5-(2-ethylhexyl)-4H-thieno(3,4-c) pyrrole-4,6-(5H)-dione (EAE) and 1,3-bis(3,3-didecyl-3,4-dihydro-2H-thieno[3,4-1)111,41-dioxepin-6-yl)-5-(2-ethylhexyl)-4H-thieno[3,4-apyrrole-4,6(5H)-dione (PAP)) and their corresponding polymers called PTAT, PEAE and PPAP were investigated and it was found that EDOT units containing monomer and polymer (EAE and PEAE) have lower oxidation potentials and lower band gap value as compared to didecyl-ProDOT and thiophene units containing monomers and polymers (PAP, TAT and PPAP, PTAT). Spectroelectrochemical investigations conducted on electrochemically obtained polymer films revealed that polymer films exhibited electrochromic behaviors: brick red to gray for PTAT, blue/violet to highly sky blue for PEAE and blue to highly light blue for PPAP in their neutral and oxidized states, respectively. Moreover, PAP was also polymerized chemically using FeC13 as an oxidizing agent. Both chemically and electrochemically obtained PPAP were found to be soluble in some organic solvents and their dichloromethane solutions can be reversibly oxidized and reduced using antimony pentachloride and hydrazine hydrate solutions, respectively.