Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Ömer Sonkaya"'
Publikováno v:
ACS Applied Bio Materials. 4:5090-5098
We disclose an interesting concept for developing heavy atom-free chemiluminogenic photosensitizers. To accomplish this, conjugates 2 and 3, which are composed of boron-dipyrromethene (BODIPY) and 2,3-dihydrophthalazine-1,4-dione units, are investiga
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4ff0768cf226df34771842a951d1d6a5
https://doi.org/10.1021/acsabm.1c00328
https://doi.org/10.1021/acsabm.1c00328
Publikováno v:
Spectrochimica Acta Part A: Molecular and Biomolecular Spectroscopy. 292:122412
Herein we describe the facile synthesis of new N-doped carbon nanoparticles (CNPs) obtained from 1,10-phenanthroline by the solvothermal method. Characterization of CNPs were carried out with transmission electron microscope (TEM), X-ray photoelectro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b8510466112fb17263bcda5d8373762d
https://doi.org/10.1016/j.saa.2023.122412
https://doi.org/10.1016/j.saa.2023.122412
Autor:
Alihan Toksoy, Ömer Sonkaya, Dilek Sadife Erkan, Rukiye Boran Gulen, Melek Pamuk Algi, Fatih Algi
Publikováno v:
Photodiagnosis and photodynamic therapy. 40
Photodynamic therapy (PDT) is a method for the treatment of cancer. Furthermore, PDT can also be used for the eradication of bacteria. The photo-sensitizing drug, a.k.a photosensitizer, is critical for the success of PDT. Although norsquaraines are a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eb6a9e40658fb06ff2bea404af84ee5e
https://pubmed.ncbi.nlm.nih.gov/36070851
https://pubmed.ncbi.nlm.nih.gov/36070851
Abstract: Aza-boron-dipyrromethenes (Aza-BODIPYs) represent an important class of chromo-phores absorbing and emitting in the near-infrared (NIR) region. They have unique optical and elec-tronic features and higher physiological and photo stability t
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e39cc7ce55172c5f8c5c64081d017d39
https://hdl.handle.net/20.500.12451/9290
https://hdl.handle.net/20.500.12451/9290
Publikováno v:
Acta Crystallographica Section E, Vol 69, Iss 6, Pp o994-o995 (2013)
In the title spiro-phosphazene derivative, C33H46N9OP3, the phosphazene and six-membered N/O rings are in flattened chair and twisted-boat conformations, respectively. The naphthalene ring system and the pyridine ring are oriented at a dihedral angle
Externí odkaz:
https://doaj.org/article/21b6852edbda4f9480dff1bf7414c095
Publikováno v:
Acta Crystallographica Section E, Vol 69, Iss 6, Pp o861-o862 (2013)
The title compound, C17H14Cl4N5OP3, is a spiro-phosphazene derivative with bulky naphthalene and pyridine rings. The phosphazene and the six-membered N/O rings are in flattened-boat and twisted-boat conformations, respectively. The naphthalene ring s
Externí odkaz:
https://doaj.org/article/4603861ba150418ebc50b13a429b45d9
WOS: 000376050700031
In this study a new monospirocyclic phosphazene derivative, 4',4',6',6'-tetrachloro-3-(2-methoxyethyl)3H,4H-spiro [1,3,2-benzoxazaphosphinine-2,2'- [1,3,5,2,4,6] triazatriphosphinine] (SP1) was synthesized from the reaction
In this study a new monospirocyclic phosphazene derivative, 4',4',6',6'-tetrachloro-3-(2-methoxyethyl)3H,4H-spiro [1,3,2-benzoxazaphosphinine-2,2'- [1,3,5,2,4,6] triazatriphosphinine] (SP1) was synthesized from the reaction
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7d33fa1930426390238c7a69b8a47b5
https://hdl.handle.net/20.500.12587/6490
https://hdl.handle.net/20.500.12587/6490
WOS: 000382941000006
Octachlorocyclotetraphosphazene, N4P4Cl8, (1) was reacted with N, N-dibenzylethylenediamine to synthesize partially substituted monospiro- (2), dispiro- (5) and tetraspirocyclotetraphosphazene (8) derivatives. The reactions
Octachlorocyclotetraphosphazene, N4P4Cl8, (1) was reacted with N, N-dibenzylethylenediamine to synthesize partially substituted monospiro- (2), dispiro- (5) and tetraspirocyclotetraphosphazene (8) derivatives. The reactions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9f04eb516e0e9df4a42986cf2272739d
https://hdl.handle.net/20.500.12587/6718
https://hdl.handle.net/20.500.12587/6718
Hokelek, Tuncer/0000-0002-8602-4382; COSUT, Bunyemin/0000-0001-6530-0205 WOS: 000277776100013 The reactions of hexachlorocyclotriphosphazene, N3P3Cl6, with N/O donor type N-alkyl or (aryl)-o-hydroxybenzylamines HO(C6H4)CH2NHR(Ar), [R(Ar) = C(CH3)(3)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::249b4b0507fef652d71a94e19376095f
https://aperta.ulakbim.gov.tr/record/23885
https://aperta.ulakbim.gov.tr/record/23885
Publikováno v:
Acta Crystallographica Section E: Structure Reports
In the title spiro-phosphazene derivative, C33H 46N9OP3, the phosphazene and six-membered N/O rings are in flattened chair and twisted-boat conformations, respectively. The naphthalene ring system and the pyridine ring are oriented at a dihedral angl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a7dca337e0bf14d9c5a68805db46664b
http://europepmc.org/articles/PMC3685126
http://europepmc.org/articles/PMC3685126