Παρακαλώ χρησιμοποιήστε αυτό το αναγνωριστικό για να παραπέμψετε ή να δημιουργήσετε σύνδεσμο προς αυτό το τεκμήριο: https://hdl.handle.net/20.500.14279/9833
Τίτλος: Identifying potential candidates for donor-acceptor copolymers on a series of 4H-1,2,6-thiadiazines: An electrochemical approach
Συγγραφείς: Economopoulos, Solon P. 
Koutentis, Panayiotis A. 
Ioannidou, Heraklidia A. 
Choulis, Stelios A. 
Major Field of Science: Natural Sciences
Field Category: Chemical Sciences
Λέξεις-κλειδιά: Electrochemistry;Light-harvesting polymers;Thiadiazines
Ημερομηνία Έκδοσης: 30-Σεπ-2013
Πηγή: Electrochimica Acta, 2013, vol. 107, pp. 448-453
Volume: 107
Start page: 448
End page: 453
Περιοδικό: Electrochimica Acta 
Περίληψη: A series of synthesized small organic molecules based on the 4H-1,2,6-thiadiazine moiety are studied using electrochemistry, to probe their potential as comonomer building blocks for solar-absorbing polymers for organic solar cells. This is the first instance of an electrochemical report for this family of heterocycles. Structure-physical property relationships are identified that can guide future synthetic efforts. Parameters that can influence the properties of the final copolymer such as the choice of electron donor comonomer and the energy level of the fullerene adduct acceptor are factored-in and discussed and the thiadiazines that can meet the requirements are singled-out.
URI: https://hdl.handle.net/20.500.14279/9833
ISSN: 00134686
DOI: 10.1016/j.electacta.2013.06.038
Rights: © Elsevier
Type: Article
Affiliation: Cyprus University of Technology 
University of Cyprus 
Publication Type: Peer Reviewed
Εμφανίζεται στις συλλογές:Άρθρα/Articles

CORE Recommender
Sorry the service is unavailable at the moment. Please try again later.
Δείξε την πλήρη περιγραφή του τεκμηρίου

SCOPUSTM   
Citations

10
checked on 9 Νοε 2023

WEB OF SCIENCETM
Citations 50

9
Last Week
0
Last month
0
checked on 29 Οκτ 2023

Page view(s)

451
Last Week
29
Last month
2
checked on 23 Φεβ 2025

Google ScholarTM

Check

Altmetric


Όλα τα τεκμήρια του δικτυακού τόπου προστατεύονται από πνευματικά δικαιώματα