Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Petia Bobadova‐Parvanova"'
Autor:
Caroline Ndung’U, Petia Bobadova-Parvanova, Daniel J. LaMaster, Dylan Goliber, Frank R. Fronczek, Maria da Graça H. Vicente
Publikováno v:
Molecules, Vol 28, Iss 12, p 4581 (2023)
The introduction of electron-withdrawing groups on 8(meso)-pyridyl-BODIPYs tends to increase the fluorescence quantum yields of this type of compound due to the decrease in electronic charge density on the BODIPY core. A new series of 8(meso)-pyridyl
Externí odkaz:
https://doaj.org/article/8985e7e0529743d7984247e8afa8d3e4
Autor:
Caroline Ndung’u, Daniel J. LaMaster, Simran Dhingra, Nathan H. Mitchell, Petia Bobadova-Parvanova, Frank R. Fronczek, Noémie Elgrishi, Maria da Graça H. Vicente
Publikováno v:
Sensors, Vol 22, Iss 14, p 5121 (2022)
Boron dipyrromethene (BODIPY) dyes bearing a pyridyl moiety have been used as metal ion sensors, pH sensors, fluorescence probes, and as sensitizers for phototherapy. A comparative study of the properties of the three structural isomers of meso-pyrid
Externí odkaz:
https://doaj.org/article/75eed804ac79421dbcf1400eb110c858
Publikováno v:
ACS Omega, Vol 3, Iss 5, Pp 5502-5510 (2018)
Externí odkaz:
https://doaj.org/article/80b9155807024456b2cf8b9c1d4780dc
Autor:
Vicente, Caroline Ndung’U, Petia Bobadova-Parvanova, Daniel J. LaMaster, Dylan Goliber, Frank R. Fronczek, Maria da Graça H.
Publikováno v:
Molecules; Volume 28; Issue 12; Pages: 4581
The introduction of electron-withdrawing groups on 8(meso)-pyridyl-BODIPYs tends to increase the fluorescence quantum yields of this type of compound due to the decrease in electronic charge density on the BODIPY core. A new series of 8(meso)-pyridyl
Autor:
Brandy-Fey C. Stratton, Angelina J. Pierre, Elizabeth A. Riser, Nathan J. Grinalds, Charles W. Edwards, Anna M. Wohlwend, Jacob S. Bauer, Rachel J. Spera, Lauren S. Pferdmenges, Kaitlyn M. Griffith, Brandon W. Hunter, Petia Bobadova-Parvanova, Cynthia S. Day, Pamela M. Lundin, Keir H. Fogarty
Publikováno v:
The Journal of Physical Chemistry A. 126:4211-4220
Amide derivatives of xanthene dyes such as rhodamine B are useful in a variety of sensing applications due to their colorimetric responses to stimuli such as acidity changes and UV light. The optical properties of these molecules can be influenced by
Autor:
Guanyu Zhang, Maodie Wang, Petia Bobadova‐Parvanova, Frank R. Fronczek, Kevin M. Smith, M. Graça H. Vicente
Publikováno v:
Chemistry – A European Journal. 28
The synthesis and reactivity of 3,8-dibromo-dodecafluoro-benzo-fused BOPHY 2 are reported, via S
Autor:
Brandy-Fey Stratton, Angelina Pierre, Elizabeth Riser, Nathan Grinalds, Charles Edwards, Anna Wohlwend, Jacob Bauer, Rachel Spera, Lauren Pferdmenges, Kaitlyn Griffith, Brandon Hunter, Petia Bobadova-Parvanova, Cynthia Day, Pamela Lundin, Keir Fogarty
Amide derivatives of xanthene dyes such as rhodamine B are useful in a variety of sensing applications due to their colorimetric responses to stimuli such as acidity changes and UV light. The optical properties of these molecules can be influenced by
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3c600fdff3b959a4ab5b0efa07ba06b7
https://doi.org/10.26434/chemrxiv-2022-f20qv-v2
https://doi.org/10.26434/chemrxiv-2022-f20qv-v2
Autor:
Petia Bobadova-Parvanova, Maodie Wang, Caroline Ndung’U, Frank R. Fronczek, Guanyu Zhang, M. Graça H. Vicente, Kevin M. Smith
Publikováno v:
Journal of Porphyrins and Phthalocyanines. 24:869-877
Three BODIPYs bearing 1,3,5,7-tetramethyl substituents and a meso-8-aryl group were synthesized and investigated, both experimentally and computationally. The presence of the 1,7-methyl groups and of ortho-substituents on the meso-8-aryl ring prevent
Autor:
Kevin M. Smith, M. Graça H. Vicente, Maodie Wang, Frank R. Fronczek, Petia Bobadova-Parvanova, Nichole E. M. Kaufman, Guanyu Zhang
Publikováno v:
European Journal of Organic Chemistry. 2020:971-977
Publikováno v:
The Journal of Organic Chemistry
A series of α-amino acid-BODIPY derivatives were synthesized using commercially available N-Boc-l-amino acids, via boron functionalization under mild conditions. The mono-linear, mono-spiro, and di-amino acid-BODIPY derivatives were obtained using a