Zobrazeno 1 - 10
of 113
pro vyhledávání: '"Alexander L, Kanibolotsky"'
Autor:
Valentin H. K. Fell, Joseph Cameron, Alexander L. Kanibolotsky, Eman J. Hussien, Peter J. Skabara
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 18, Iss 1, Pp 944-955 (2022)
A novel π-conjugated molecule, EtH-T-DI-DTT is reported, which is fused, rigid, and planar, featuring the electron-rich dithieno[3,2-b:2’,3’-d]thiophene (DTT) unit in the core of the structure. Adjacent to the electron-donating DTT core, there a
Externí odkaz:
https://doaj.org/article/8bde1481f79f47039d028173b3a879fd
Autor:
Saadeldin E. T. Elmasly, Luca Guerrini, Joseph Cameron, Alexander L. Kanibolotsky, Neil J. Findlay, Karen Faulds, Peter J. Skabara
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 14, Iss 1, Pp 2186-2189 (2018)
A novel methodology towards fabrication of multilayer organic devices, employing electrochemical polymer growth to form PEDOT and PEDTT layers, is successfully demonstrated. Moreover, careful control of the electrochemical conditions allows the degre
Externí odkaz:
https://doaj.org/article/804ce7eaec894dd8b744c2bf7ce2e35b
Publikováno v:
Advanced Materials.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5614a18bd4256bd12a29db0cc22a4a5c
https://doi.org/10.1002/adma.202302259
https://doi.org/10.1002/adma.202302259
Publikováno v:
Arkivoc. 2021:268-314
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f15a9d4cd0a15b924bea16f185d1adb4
https://doi.org/10.24820/ark.5550190.p011.611
https://doi.org/10.24820/ark.5550190.p011.611
Polythiophene and oligothiophene systems modified by TTF electroactive units for organic electronics
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 11, Iss 1, Pp 1749-1766 (2015)
The aim of this review is to give an update on current progress in the synthesis, properties and applications of thiophene-based conjugated systems bearing tetrathiafulvalene (TTF) units. We focus mostly on the synthesis of poly- and oligothiophenes
Externí odkaz:
https://doaj.org/article/aa7e321fadaa4fe19bdc95e98415c72c
Autor:
Rupert G. D. Taylor, Joseph Cameron, Iain A. Wright, Neil Thomson, Olena Avramchenko, Alexander L. Kanibolotsky, Anto R. Inigo, Tell Tuttle, Peter J. Skabara
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 11, Iss 1, Pp 1148-1154 (2015)
Two novel tetrathiafulvalene (TTF) containing compounds 1 and 2 have been synthesised via a four-fold Stille coupling between a tetrabromo-dithienoTTF 5 and stannylated thiophene 6 or thiazole 4. The optical and electrochemical properties of compound
Externí odkaz:
https://doaj.org/article/cf1377eeadc846f8adef00ab5ebe996c
Autor:
Clara Orofino-Pena, Diego Cortizo-Lacalle, Joseph Cameron, Muhammad T. Sajjad, Pavlos P. Manousiadis, Neil J. Findlay, Alexander L. Kanibolotsky, Dimali Amarasinghe, Peter J. Skabara, Tell Tuttle, Graham A. Turnbull, Ifor D. W. Samuel
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 10, Iss 1, Pp 2704-2714 (2014)
Star-shaped conjugated systems with varying oligofluorene arm length and substitution patterns of the central BODIPY core have been synthesised, leading to two families of compounds, T-B1–T-B4 and Y-B1–Y-B4, with T- and Y-shaped motifs, respectiv
Externí odkaz:
https://doaj.org/article/9ffd7b35fbd0481c89b95e9847eaa5ed
Autor:
Neil Thomson, Alexander L. Kanibolotsky, Joseph Cameron, Tell Tuttle, Neil J. Findlay, Peter J. Skabara
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 1243-1251 (2013)
Oligofluorene-functionalised truxenes containing perfluorohexylthiophene units at the terminal positions on the arms were synthesised, and their optical and electrochemical properties were investigated to determine the effect that the perfluorohexylt
Externí odkaz:
https://doaj.org/article/071707a167ab40e9bfe8739b3cd501c2
Autor:
Alexander L. Kanibolotsky, Simon J. Coles, Iain A. Wright, Lethy Krishnan Jagadamma, Peter J. Skabara, Peter N. Horton, Rupert G. D. Taylor, Ifor D. W. Samuel, Muhammad T. Sajjad
Publikováno v:
Sustainable Energy & Fuels. 3:2087-2099
Authors thank the EPSRC for funding under grants EP/L012200/1 and EP/L012294/1. A new dual-chain oligothiophene-based organic semiconductor, EH-5T-TTC, is presented. The molecule contains two conjugated chains linked by a fused tetrathiocin core. X-r
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::023f825f85de129e9e716391a2f05dcf
https://doi.org/10.1039/c9se00343f
https://doi.org/10.1039/c9se00343f
Autor:
Olga M. Zarechnaya, Alexander L. Kanibolotsky, Vasilii A. Mikhailov, Eugenii Yu Belov, Nikolai I. Burakov, Aleksei A. Anisimov
Dihalogens readily interact with trimethylamine-N-oxide under ambient conditions. Accordingly, herein, stable 1 : 1 adducts were obtained in the case of iodine chloride and iodine bromide. The crystal and molecular structure of the trimethylamine-N-o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ec19305125ef0d9f441a7e1232f07545
https://eprints.gla.ac.uk/234029/1/234029.pdf
https://eprints.gla.ac.uk/234029/1/234029.pdf
