Zobrazeno 1 - 10
of 109
pro vyhledávání: '"Pakkirisamy Thilagar"'
Publikováno v:
Frontiers in Chemistry, Vol 8 (2020)
We report a simple and novel molecular design strategy to enhance rISC in boron-based donor–acceptor systems to achieve improved delayed fluorescence characteristics. Dianthrylboryl ((An)2B)-based aryl aminoboranes 1 (donor: phenothiazine) and 2 (d
Externí odkaz:
https://doaj.org/article/4e94e762449142bdb7176b195cfc6dfd
Publikováno v:
The Journal of Physical Chemistry C. 127:9918-9930
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f93fa1f6ea37108d7dbe357344ceef59
https://doi.org/10.1021/acs.jpcc.3c01995
https://doi.org/10.1021/acs.jpcc.3c01995
Publikováno v:
Inorganic Chemistry. 62:1122-1134
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b6185abdf003f4e355c7629d82f2d7da
https://doi.org/10.1021/acs.inorgchem.2c03386
https://doi.org/10.1021/acs.inorgchem.2c03386
Autor:
Satyam Jena, Jusaina Eyyathiyil, Santosh Kumar Behera, Maho Kitahara, Yoshitane Imai, Pakkirisamy Thilagar
Publikováno v:
Chemical Science. 13:5893-5901
We report the design and synthesis of a series of room temperature phosphorescent phosphoramides TPTZPO, TPTZPS, and TPTZPSe with a donor (phenothiazine)-acceptor (P = X, X = O, S, and Se) architecture. All the compounds show structureless fluorescen
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8352c78091e5d6f14fdd331514b83d27
https://doi.org/10.1039/d2sc00990k
https://doi.org/10.1039/d2sc00990k
Publikováno v:
Journal of Materials Chemistry C. 10:9124-9131
Ultralong room temperature phosphorescence of simple triarylphosphine oxides is reported. The lone pair electrons on the P in triarylphosphines facilitate faster intersystem crossing than those on the O of the P=O moiety in triarylphosphine oxides.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ddea0c4fa829aea936caae7d87222642
https://doi.org/10.1039/d2tc01318e
https://doi.org/10.1039/d2tc01318e
Autor:
Upendra K. Pandey, Pakkirisamy Thilagar, Christine K. Luscombe, Samir Kumar Sarkar, Lauren J. Kang
Publikováno v:
Solar Energy. 230:242-249
A new X-type, structurally twisted, highly soluble TAB-BODIPY based electron acceptor (BDY) is designed and synthesized. Organic solar devices are fabricated using poly(3-hexylthiophene-2,5-diyl) (P3HT) as donor polymer and BDY as an electron accepto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ce4d98050b3adfeab4bd6b3e6c759ece
https://doi.org/10.1016/j.solener.2021.10.048
https://doi.org/10.1016/j.solener.2021.10.048
Autor:
Rajendra Prasad Nandi, Subhajit Ghosh, Krishnan Venkatasubbaiah, Dipak Kumbhar, Pakkirisamy Thilagar
Publikováno v:
ChemPhotoChem. 6
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dfb139dfeacdf0c20c94f06e9534f5f1
https://doi.org/10.1002/cptc.202200026
https://doi.org/10.1002/cptc.202200026
Publikováno v:
The Journal of organic chemistry. 87(6)
Herein, we report the design and synthesis of far-red emissive boryl-thiophene-BODIPY triads
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b36d6ef572def1011c803987b223b93
https://pubmed.ncbi.nlm.nih.gov/35254826
https://pubmed.ncbi.nlm.nih.gov/35254826
Publikováno v:
The Journal of Physical Chemistry B. 124:8896-8903
Three new triads [bis(mesityl)boryl (Mes2B)–vinylbithiophene–BODIPY] bearing zero (1), two (2), and four (3) methyl groups on the BODIPY core are synthesized, and their optical properties are repor...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::20a845a10c6a01f21015afbe60f9443f
https://doi.org/10.1021/acs.jpcb.0c07463
https://doi.org/10.1021/acs.jpcb.0c07463
Publikováno v:
The Journal of Physical Chemistry B. 124:5393-5406
We study the effect of molecular conformation on the electronic coupling between the donor amines and acceptor 1,8-naphthalimide (NPI) in a series of D-A systems 1-4 (A = NPI; D = phenothiazine, phenoxazine, carbazole, diphenylamine, respectively, fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a4e358236b1fc19e5818eec64f844129
https://doi.org/10.1021/acs.jpcb.0c04115
https://doi.org/10.1021/acs.jpcb.0c04115