Synthesis and characterization of 5-(4-carboxyphenylspermine)-10,15,20-triphenylporphyrin

2020 ◽  
Vol 24 (05n07) ◽  
pp. 802-808
Author(s):  
Chiara M.A. Gangemi ◽  
Rosalba Randazzo ◽  
Massimiliano Gaeta ◽  
Cosimo G. Fortuna ◽  
Maria E. Fragalà ◽  
...  
Keyword(s):  
Fluorescence Spectroscopy ◽  
Photophysical Properties ◽  
Soret Band ◽  
Fluorescence Band ◽  
Synthesis And Characterization ◽  
Acidic Solutions ◽  
Protonation Equilibria ◽  
The Core ◽  
Aggregation Processes

We synthetized and characterized a mono spermine porphyrin derivative by NMR, UV-vis and fluorescence spectroscopy. The photophysical properties and the protonation equilibria of 5-(4-carboxyphenylspermine)-10,15,20-triphenylporphyrin have been investigated, showing that porphyrin does not aggregate in acidic solutions, differently from what occurs as soon as the core of the porphyrin is deprotonated. These aggregation processes have been detected by the rising of new fluorescence band and a significant splitting of the Soret band.

scholarly journals Synthesis and Characterization of a Multifunctional Conjugated Polymer

2018 ◽  
Vol 2018 ◽  
pp. 1-9 ◽  
Author(s):  
Emerson C. G. Campos ◽  
Cristiano Zanlorenzi ◽  
Bruno F. Nowacki ◽  
Gabriela M. Miranda ◽  
Denis A. Turchetti ◽  
...  
Keyword(s):  
Conjugated Polymer ◽  
Molar Mass ◽  
Photophysical Properties ◽  
Gel Permeation Chromatography ◽  
Thermal Characterization ◽  
Polymer Structure ◽  
Synthesis And Characterization ◽  
Metallic Ions ◽  
Scanning Calorimetry

This work reports the synthesis and characterization of a conjugated polymer based on fluorene and terpyridine, namely, poly[(9,9-bis(3-((S)-2-methylbutylpropanoate))fluorene-alt-6,6′-(2,2′:6′,2′′-terpyridin-6-yl)] (LaPPS71). The structure was characterized by 1H and 13C nuclear magnetic resonance (NMR) and Fourier-transform infrared (FTIR) spectroscopy. The molar mass was measured by gel permeation chromatography (GPC). As thermal characterization, the glass transition temperature (Tg) was measured by differential scanning calorimetry (DSC). The polymer structure contains two sites capable of complexation with metallic ions, affording the possibility of obtainment of independent or electronically coupled properties, depending on the complexation site. The photophysical properties were fully explored in solution and solid state, presenting ideal results for the preparation of various metallopolymers, in addition to potential application as a metamaterial, due to the presence of the chiral center in the side chains of the polymer.

New peripherally substituted lutetium mono and bis phthalocyanines: Synthesis and comparative photophysical and photochemical properties

2019 ◽  
Vol 23 (11n12) ◽  
pp. 1542-1550
Author(s):  
Nagihan Kocaağa ◽  
Öznur Dülger Kutlu ◽  
Ali Erdoğmuş
Keyword(s):  
Mass Spectrometry ◽  
Photodynamic Therapy ◽  
Singlet Oxygen ◽  
Photophysical Properties ◽  
Quantum Yields ◽  
Synthesis And Characterization ◽  
Type Ii ◽  
H Nmr ◽  
Photochemical Properties

In this study, the synthesis and characterization of mono-(phthalocyaninato) lutetium(III) (1-Cl and 1-F) [Lu[Formula: see text](AcO)(Pc)] (Pc [Formula: see text] phthalocyaninato, AcO [Formula: see text] acetate) and bis-(phthalocyaninato) lutetium(III) (2-Cl and 2-Br) [Lu[Formula: see text]Pc[Formula: see text]] bearing halogenated (F, Cl and Br) phenoxy–phenoxy groups are described and verified by IR, [Formula: see text]H-NMR, UV-vis and mass spectrometry. Photochemical and photophysical properties of 1-F, 1-Cl 2-Cl and 2-Br in DMSO are also presented. A comparison between photophysical and photochemical parameters of mono and bis derivatives showed that mono phthalocyanines are better photosensitizers than bis phthalocyanines. Photophysical and photochemical properties of phthalocyanines are very useful for photodynamic therapy applications. Singlet oxygen quantum yields [Formula: see text] give an indication of the potential of the complexes as photosensitizers in photodynamic therapy applications. The chloro, fluoro, bromo-phenoxy–phenoxy substituted mono-(phthalocyaninato) lutetium(III) complexes (1-Cl and 1-F) gave good singlet oxygen quantum yields (from 0.86 to 0.80) in DMSO. Thus, these complexes show potential as Type II photosensitizers for PDT of cancer.

Towards the Synthesis of Mono- and Bi-Functional Amphiphilic Oligothiophenes: Organic Materials for Opto-Electronic Applications

1999 ◽  
Vol 561 ◽  
Author(s):  
R.C. Advincula ◽  
S. Inaoka ◽  
M. Park ◽  
D. Phillips ◽  
D.M. Shin
Keyword(s):  
Physical Properties ◽  
Ultrathin Films ◽  
Organic Materials ◽  
Photophysical Properties ◽  
Electronic Devices ◽  
Synthesis And Characterization ◽  
Important Class ◽  
Maldi Tof Ms ◽  
Tof Ms

ABSTRACTIn this report, we describe our initial synthesis and characterization of mono-functional and bi-functional dibromoalkyl oligothiophenes to achieve amphiphilicity and telechelic functionality. Oligothiophenes are an important class of organic materials for opto-electronic devices and display applications. We have mono-functionalized oligothiophenes by the synthesis of a quinquethiophene bromoalkyl derivative. A bi-functional sexithiophene was derived primarily by the symmetrical coupling of terthiophene derivatives. Both were synthesized using Grignard coupling and lithiation reaction methodologies. UV-Vis, IR, NMR, MALDI-TOF-MS, and DSC confirmed the structure and physical properties of the oligomers. In addition, we have also synthesized an amphiphilic diamine derivative from the reaction of hexamethylenediamine with a bromoalkyl terthiophene derivative. Using photoluminescence, the photophysical properties of the oligomers were found to be that of typical oligothiophenes. Processing as ultrathin films for devices is currently being investigated.

scholarly journals Synthesis and Characterization of Acridinium Dyes for Photoredox Catalysis

Synlett ◽  
2019 ◽  
Vol 30 (07) ◽  
pp. 827-832 ◽  
Author(s):  
Alexander White ◽  
Leifeng Wang ◽  
David Nicewicz
Keyword(s):  
Photophysical Properties ◽  
Direct Conversion ◽  
Systematic Investigation ◽  
Synthetic Methods ◽  
Synthesis And Characterization ◽  
Substitution Effects ◽  
Photoredox Catalysis ◽  
Methods Development

Photoredox catalysis is a rapidly evolving platform for synthetic methods development. The prominent use of acridinium salts as a sustainable option for photoredox catalysts has driven the development of more robust and synthetically useful versions based on this scaffold. However, more complicated syntheses, increased cost, and limited commercial availability have hindered the adoption of these catalysts by the greater synthetic community. By utilizing the direct conversion of a xanthylium salt into the corresponding acridinium as the key transformation, we present an efficient and scalable preparation of the most synthetically useful acridinium reported to date. This divergent strategy also enabled the preparation of a suite of novel acridinium dyes, allowing for a systematic investigation of substitution effects on their photophysical properties.

Synthesis and Characterization of Comb-Type Grafted Hydrogels

2012 ◽  
Vol 602-604 ◽  
pp. 1274-1284
Author(s):  
Ping Zhang ◽  
Shi Pu Li ◽  
Xin Yu Wang ◽  
Hong Lian Dai
Keyword(s):  
Aqueous Solution ◽  
Fluorescence Spectroscopy ◽  
Lower Critical Solution Temperature ◽  
Ammonium Persulfate ◽  
Solution Temperature ◽  
Synthesis And Characterization ◽  
Critical Solution Temperature

The grafted hydrogels of N-isopropylacrylamide (IPAAm) with 2-hydroxyethylacrylate (HEA) was prepared in an aqueous solution using ammonium persulfate (APS) and N,N,N’,N’-tetramethylethylene diamine (TEMED) as an accelerator. Lower critical solution temperature (LCST) and swelling ratios were measured as a function of temperature. The properties of the hydrogels contained pyrenyl probe in water were investigated by fluorescence spectroscopy.

Synthesis and Characterization of Luminescent Rod-Coil Poly[2,7-(9,9- Dihexylfluorene)] - Block-Poly(2-(Dimethylamino) Ethyl Methacrylate) by Atom Transfer Radical Polymerization

2008 ◽  
Vol 47-50 ◽  
pp. 642-645
Author(s):  
Yang Yen Yu ◽  
Wen Chen Chien ◽  
Chia Liang Tsai
Keyword(s):  
Atom Transfer Radical Polymerization ◽  
Radical Polymerization ◽  
Photophysical Properties ◽  
Mixed Solvents ◽  
Solvent System ◽  
Synthesis And Characterization ◽  
Photoluminescence Properties ◽  
Ethyl Methacrylate ◽  
Large Compound

The synthesis, morphology, and photophysical properties of Poly[2,7-(9,9-dihexyl fluorene)]- block-poly(2-(Dimethylamino) ethyl methacrylate) (PF-b-PDMAEMA) copolymers in various mixed solvents, i.e., THF/MeOH, DMF/MeOH, and 1,4-Dioxane/MeOH, with methanol contents of 0, 10, 25, 50, 75, 90 vol.% were reported. TEM images showed that different aggregate morphologies of PF-b-PDMAEMA, including spherical and large compound micelles, cylinder, nanorods, long stick-like structure, could be prepared by introducing different amount of methanol into the copolymer/solvent system. The results indicated that aggregate morphologies of PF-b-PDMAEMA, which obtained from various coil lengths and mixed solvents, had a great influenced on the optical and photoluminescence properties of the prepared PF-b-PDMAEMA copolymers.

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