One-Step Synthesis of Indolizino[3,4,5-ab]isoindoles by Manganese(I)-Catalyzed C–H Activation: Structural Studies and Photophysical Properties

2022 ◽  
Author(s):  
Sara Cembellin ◽  
Ivan Maisuls ◽  
Constantin Gabriel Daniliuc ◽  
Helena Osthues ◽  
Nikos Doltsinis ◽  
...  
Keyword(s):  
Photophysical Properties ◽  
Regioselective Synthesis ◽  
Luminescence Properties ◽  
Structural Studies ◽  
Step Procedure ◽  
One Step

Herein, a regioselective synthesis of indolizino[3,4,5-ab]isoindoles (INIs), a valuable class of heterocycles with interesting luminescence properties, is described using manganese(I)-catalyzed C−H activation. The reported transformation proceeds in a one-step procedure...

A quick one-step synthesis of luminescent gold nanospheres

Soft Matter ◽  
2020 ◽  
Vol 16 (48) ◽  
pp. 10865-10868
Author(s):  
Angela Candreva ◽  
Giuseppe Di Maio ◽  
Massimo La Deda
Keyword(s):  
Visible Spectrum ◽  
Luminescence Properties ◽  
Gold Nanospheres ◽  
Step Procedure ◽  
Wide Range ◽  
One Step ◽  
Application Fields

Luminescent gold nanospheres emissive in a wide range of the visible spectrum have been synthesized by a quick one-step procedure; the coexistence of the plasmonic and luminescence properties makes them useful in various application fields.

Synthesis and photophysical properties of benzo[c]phenanthrene derivatives

2021 ◽  
Vol 18 ◽  
Author(s):  
Amira K. Hajri ◽  
Marzough A. Albalawi ◽  
Souad A. Moussa ◽  
Faouzi Aloui
Keyword(s):  
Small Molecules ◽  
Photophysical Properties ◽  
Stokes Shift ◽  
Visible Spectrum ◽  
Strong Emission ◽  
Step Procedure ◽  
Polycyclic Aromatic ◽  
One Step ◽  
Conjugated Compounds ◽  
Stokes Shifts

Background: Three polycyclic aromatic hydrocarbons derived from benzo[c]phenanthrene have been synthesized through a one-step procedure involving palladium Suzuki coupling and are characterized by 1 H and 13C NMR, MS and HRMS spectroscopies. Methods: UV-vis absorption and fluorescence properties of these π-conjugated compounds have been evaluated in solutions and strong emission in the blue region of the visible spectrum was noted. Results: The optical spectra of these small polycyclic aromatic compounds are unusual because absorption is entirely in the UV region (λmax = 281-285 nm), yet fluorescence occurs at 410-422 nm. Conclusion: This equates to a Stokes shift of 1.32-1.39 eV (10756-11256 cm−1 ) and is among the large Stokes shifts that have been reported for small molecules, making them promising candidates for optoelectronic applications.

scholarly journals Electrochromic Performance and Capacitor Performance of α-MoO3 Nanorods Fabricated by a One-Step Procedure

Coatings ◽  
2021 ◽  
Vol 11 (7) ◽  
pp. 783
Author(s):  
Ying Duan ◽  
Chen Wang ◽  
Jian Hao ◽  
Yang Jiao ◽  
Yanchao Xu ◽  
...  
Keyword(s):  
Growth Parameters ◽  
Average Diameter ◽  
Fast Response ◽  
Cycle Stability ◽  
Electrochromic Devices ◽  
Step Procedure ◽  
One Step ◽  
Supercapacitor Performance ◽  
First Time ◽  
Prepared Nanorods

In this paper, we propose for the first time the synthesis of α-MoO3 nanorods in a one-step procedure at mild temperatures. By changing the growth parameters, the microstructure and controllable morphology of the resulting products can be customized. The average diameter of the as-prepared nanorods is about 200 nm. The electrochromic and capacitance properties of the synthesized products were studied. The results show that the electrochromic properties of α-MoO3 nanorods at 550 nm have 67% high transmission contrast, good cycle stability and fast response time. The MoO3 nanorods also exhibit a stable supercapacitor performance with 98.5% capacitance retention after 10,000 cycles. Although current density varies sequentially, the nanostructure always exhibits a stable capacitor to maintain 100%. These results indicate the as-prepared MoO3 nanorods may be good candidates for applications in electrochromic devices and supercapacitors.

Regioselective synthesis of functionalized [1,6]-naphthyridines by KF/basic alumina as a recyclable catalyst and a brief study of their photophysical properties

2016 ◽  
Vol 46 (17) ◽  
pp. 1461-1476 ◽  
Author(s):  
Sibaji Nandi ◽  
Mullah Muhaiminul Islam ◽  
Mithu Saha ◽  
Sivaprasad Mitra ◽  
Snehadrinarayan Khatua ◽  
...  
Keyword(s):  
Photophysical Properties ◽  
Recyclable Catalyst ◽  
Regioselective Synthesis ◽  
Basic Alumina

One-step procedure for the preparation of tertiary .alpha.-ketols from the corresponding ketones

1968 ◽  
Vol 33 (8) ◽  
pp. 3294-3297 ◽  
Author(s):  
J. N. Gardner ◽  
F. E. Carlon ◽  
O. Gnoj
Keyword(s):  
Step Procedure ◽  
One Step

Nitroxide radicals appended to phthalonitriles: synthesis, structural characterization and photophysical properties

2021 ◽  
Vol 77 (3) ◽  
pp. 137-143
Author(s):  
Ismail Fidan ◽  
Emel Onal ◽  
Catherine Hirel
Keyword(s):  
Magnetic Measurements ◽  
Photophysical Properties ◽  
Nucleophilic Aromatic Substitution ◽  
Structural Studies ◽  
Aromatic Substitution ◽  
Nitronyl Nitroxide ◽  
X Ray Diffraction ◽  
X Ray ◽  
Microwave Assisted ◽  
Ft Ir

The syntheses of 4-[4-(4,4,5,5-tetramethyl-2-imidazoline-3-oxide-1-oxyl-2-yl)phenoxy]phthalonitrile (3, C21H19N4O3) and 4-[4-(4,4,5,5-tetramethyl-2-imidazoline-1-oxyl-2-yl)phenoxy]phthalonitrile (4) were carried out by microwave-assisted nucleophilic aromatic substitution of 4-nitrophthalonitrile (2) by the pre-formed 2-(4-hydroxyphenyl)-4,4,5,5-tetramethyl-2-imidazoline-3-oxide-1-oxyl (1). Compounds 3 and 4 were characterized unambiguously by a rich array of analyses, such as melting point, FT–IR, MALDI–TOF MS, elemental analysis, UV–Vis, CV, EPR, magnetic measurements and single-crystal X-ray diffraction. Structural studies demonstrate that the C—H...X and C—X...π (X = O and N) interactions in the radical nitronyl nitroxide groups play an important role in the assembly of the crystal structures. Moreover, cyclic voltammetry analyses show that the phthalonitrile substituent retains the redox properties of the Ullman radicals.

An innovative and efficient method to synthesize meloxicam in one-step procedure with respect to the green chemistry

2018 ◽  
Vol 16 (3) ◽  
pp. 501-509 ◽  
Author(s):  
Pierrick Dufrénoy ◽  
Alina Ghinet ◽  
Marie Hechelski ◽  
Adam Daïch ◽  
Christophe Waterlot
Keyword(s):  
Green Chemistry ◽  
Efficient Method ◽  
Step Procedure ◽  
One Step

scholarly journals An effective GC method for the determination of the fatty acid composition in silkworm pupae oil using a two-step methylation process

2015 ◽  
Vol 80 (1) ◽  
pp. 9-20 ◽  
Author(s):  
Jun Wang ◽  
Weiwei Wu ◽  
Xudong Wang ◽  
Min Wang ◽  
Fuan Wu
Keyword(s):  
Fatty Acid Composition ◽  
Fatty Acid ◽  
Acid Composition ◽  
Methyl Esters ◽  
Superior Performance ◽  
Step Procedure ◽  
Silkworm Pupae ◽  
Chromatographic Procedure ◽  
One Step ◽  
Synthesis Yield

In search of an accurate and effective method to determine fatty acid composition in silkworm pupae oils, five methylation methods were evaluated for use in the gas chromatographic (GC) quantitation of fatty acid methyl esters (FAMEs), including one-step esterification catalyzed by an acidic (H2SO4 and BF3) or alkali catalyst (KOH and NaOCH3) and a two-step procedure catalyzed successively by KOH and H2SO4. These methods were comparatively adopted to quantify FAMEs in silkworm pupae oil using GC-MS and GC and then validate their precision, stability and average recovery rates. The results indicated that compared with the other four methyl esterification methods, two-step methylation effectively improves the synthesis yield of FAMEs, conserves agents, and eliminates the usage of potential harmful reagents. The proposed GC method has been validated, shows good accuracy and precision, and has been applied successfully to the quantification of FAMEs in several varieties of silkworm pupae oils. The short analytical run time leads to low costs and a fast chromatographic procedure. In summary, two-step pretreatment had superior performance, providing technical references for the determination and analysis of fatty acids in other oils.

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