Karthigha, S.’s team published research in Journal of Physics and Chemistry of Solids in 114 | CAS: 606-55-3

Journal of Physics and Chemistry of Solids published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C12H14IN, Safety of 1-Ethyl-2-methylquinolin-1-ium iodide.

Karthigha, S. published the artcileSynthesis, growth, crystal structure, optical and third order nonlinear optical properties of quinolinium derivative single crystal: PNQI, Safety of 1-Ethyl-2-methylquinolin-1-ium iodide, the publication is Journal of Physics and Chemistry of Solids (2018), 133-140, database is CAplus.

An organic quinolinium derivative nonlinear optical (NLO) crystal, 1-ethyl-2-[2-(4-nitro-phenyl)-vinyl]-quinolinium iodide (PNQI) was synthesized and successfully grown by slow evaporation solution growth technique. Formation of a crystalline compound was confirmed by single crystal X-ray diffraction. The quinolinium compound PNQI crystallizes in the triclinic crystal system with a centrosym. space group of P-1 symmetry. The mol. structure of PNQI was confirmed by 1H NMR and 13C NMR spectral studies. The thermal properties of the crystal have been investigated by thermogravimetric (TG) and differential scanning calorimetry (DSC) studies. The optical characteristics obtained from UV-Vis-NIR spectral data were described and the cut-off wavelength observed at 506 nm. The etching study was performed to analyze the growth features of PNQI single crystal. The third order NLO properties such as nonlinear refractive index (n2), nonlinear absorption coefficient (β) and nonlinear susceptibility (χ (3)) of the crystal were investigated using Z-scan technique at 632.8 nm of He-Ne laser.

Journal of Physics and Chemistry of Solids published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C12H14IN, Safety of 1-Ethyl-2-methylquinolin-1-ium iodide.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Simon, P.’s team published research in Sensors and Actuators, B: Chemical in 90 | CAS: 606-55-3

Sensors and Actuators, B: Chemical published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C6H13BO3, Computed Properties of 606-55-3.

Simon, P. published the artcileNew NIR dyes for ammonia sensing, Computed Properties of 606-55-3, the publication is Sensors and Actuators, B: Chemical (2003), 90(1-3), 9-14, database is CAplus.

Three series of new cyanine dyes were synthesized and the visible-NIR spectra of the dyes were measured and interpreted by semi-empirical methods of quantum chem. As a basic building block for the synthesis, 4-(dimethylaminomethylene)-5-oxo-2-furfurylidenedimethyliminium perchlorate (I) was used. The dyes were prepared by condensing I with appropriate salts. The tests for sensitivity to ammonia showed that mono-substituted dyes III are reversibly sensitive to ammonia in ethanol solutions The dyes exhibit a peak at 620-680 nm arising from the interaction with ammonia and, hence, these dyes are promising as chem. transducers for distributed fiber-optic ammonia sensors.

Sensors and Actuators, B: Chemical published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C6H13BO3, Computed Properties of 606-55-3.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

El-Aal, R. M. Abd’s team published research in Journal of the Chinese Chemical Society (Taipei) in 47 | CAS: 606-55-3

Journal of the Chinese Chemical Society (Taipei) published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C12H14IN, COA of Formula: C12H14IN.

El-Aal, R. M. Abd published the artcileSynthesis, absorption spectra studies and biological activity of some novel conjugated dyes, COA of Formula: C12H14IN, the publication is Journal of the Chinese Chemical Society (Taipei) (2000), 47(2), 389-395, database is CAplus.

Novel monomethine, dimethine, and tetramethine cyanine dyes were prepared as conjugated dyes. Such dyes incorporated coumarin and/or quinoline derivatives These dyes were synthesized to study their spectral behavior, solvatochromism, and biol. activity. These dyes were characterized by elemental anal. and IR, 1H NMR, and mass spectra.

Journal of the Chinese Chemical Society (Taipei) published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C12H14IN, COA of Formula: C12H14IN.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Abed El-Aal, R. M.’s team published research in Dyes and Pigments in 54 | CAS: 606-55-3

Dyes and Pigments published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C12H14IN, Computed Properties of 606-55-3.

Abed El-Aal, R. M. published the artcileSynthesis and photophysics in organic solvents of mesosubstituted pentamethine and related metal complexes cyanine dyes, Computed Properties of 606-55-3, the publication is Dyes and Pigments (2002), 54(2), 121-129, database is CAplus.

The reaction in a ratio of 1 mol of diacetylchloromethane with 1 mol of heterocyclic nitrogen bases afforded N-substituted heterocyclidinium ylide halides. Reaction at a ratio of 1 mol of ylides with 2 and 3 mol of 2(4)-methylheterocyclic quaternary salts in basic catalyst afforded meso-substituted pentamethine and monomethine meso-substituted pentamethine cyanine dyes, resp. Reaction of equimolar ratios of metal chloride adducts of the ylides with equi- (bi)molar ratios of 2(4)-methylheterocyclic quaternary salts in basic medium afforded asym. (sym.) meso-substituted mono- (bis)monomethine metal complex cyanine dyes. Elemental analyses and IR and 1H NMR spectral data confirmed the structures of the newly synthesized compounds The electronic absorption spectra of these dyes in ethanol and their photophysics in different solvents are discussed.

Dyes and Pigments published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C12H14IN, Computed Properties of 606-55-3.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Abd El-Aal, R. M.’s team published research in Dyes and Pigments in 66 | CAS: 606-55-3

Dyes and Pigments published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C12H14IN, Safety of 1-Ethyl-2-methylquinolin-1-ium iodide.

Abd El-Aal, R. M. published the artcileThe use of oxonium salts in the synthesis of mono-, β-substituted dimethine and styryl cyanine dyes, Safety of 1-Ethyl-2-methylquinolin-1-ium iodide, the publication is Dyes and Pigments (2005), 66(3), 201-209, database is CAplus.

Pyrazolopyrylium perchlorate salt derivatives were obtained from the reaction of 5-chloro-4-formyl-3-methyl-1-phenylpyrazole with methylphenylpyrazolone, 4(2-propenyl)-1,6-ene-2-cyclohexanone, and cyclohexanone. Reaction of the salts with 2(4)-Me-substituted heterocyclic quaternary salts gave the pyrazolopyrylium 4[2(4)]-monomethine cyanine dyes. Meanwhile, reaction with amide compounds gives intermediate compounds which when reacted with 2(4)-Me-substituted heterocyclic quaternary salts gave the pyrazolopyrylium 4[2(4)]-β-substituted dimethines. Reaction of the intermediate compounds with various aromatic aldehydes followed by the reaction with 2-methylquinolinium ethiodide gave bis styryl cyanine dyes. Elemental analyses and visible absorption, IR, 1H NMR, and mass spectra established the structures of these compounds The relationship between the structure and properties of these dyes is discussed.

Dyes and Pigments published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C12H14IN, Safety of 1-Ethyl-2-methylquinolin-1-ium iodide.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Koenigstein, Christian’s team published research in Journal of Photochemistry and Photobiology, A: Chemistry in 84 | CAS: 606-55-3

Journal of Photochemistry and Photobiology, A: Chemistry published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C12H14IN, Recommanded Product: 1-Ethyl-2-methylquinolin-1-ium iodide.

Koenigstein, Christian published the artcileOrigin of the high-energy emission of 1,1′-diethyl-2,2′-cyanine dye, Recommanded Product: 1-Ethyl-2-methylquinolin-1-ium iodide, the publication is Journal of Photochemistry and Photobiology, A: Chemistry (1994), 84(3), 245-8, database is CAplus.

In addition to the yellow emission ascribed to the J aggregates of 1,1′-diethyl-2,2′-cyanine, this compound also exhibits a high-energy emission around 400 nm in dilute aqueous solutions (c<10-3 mol l-1). It was found using time-resolved emission measurements that protonation of 1,1′-diethyl-2,2′-cyanine is responsible for this emission. At pH<4, the excited state protolytic reaction competes with ground state protonation. Both pathways give the same excited species, luminescing at 400 nm. The non-protonated form shows only weak fluorescence. The excited state lifetime of the protonated form is 4.5 ns.

Journal of Photochemistry and Photobiology, A: Chemistry published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C12H14IN, Recommanded Product: 1-Ethyl-2-methylquinolin-1-ium iodide.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Ichijo, Keisuke’s team published research in ACS Omega in 6 | CAS: 606-55-3

ACS Omega published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C12H14IN, Product Details of C12H14IN.

Ichijo, Keisuke published the artcileCrystal Structures and Optical Properties of Cyanine Dyes Depending on Various Counter Anions, Product Details of C12H14IN, the publication is ACS Omega (2021), 6(42), 28421-28431, database is CAplus and MEDLINE.

In this study, cyanine cations with various counter anions were prepared as examples of ionic materials constructed using charged π-conjugated systems. A series of ion pairs was obtained by anion exchange reactions using iodide salts of carbocyanine dyes. The optical properties were measured by UV/vis absorption and fluorescence spectroscopy; measurements performed in CHCl3 (less-polar solvent) were altered by the influence of the counter anions. The packing structures of nine crystals were determined by single-crystal X-ray anal. Moreover, the locations of the anions relative to the cations were stabilized by hydrogen bonding and categorized into two types. In addition, delocalization of the neg. charge of the anions on cyanine cations was explained by d. functional theory calculations Furthermore, it was concluded that the stack formation of cyanine cations depends on the size and structure of the anions.

ACS Omega published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C12H14IN, Product Details of C12H14IN.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Bajorek, Agnieszka’s team published research in Dyes and Pigments in 82 | CAS: 606-55-3

Dyes and Pigments published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C12H14IN, Synthetic Route of 606-55-3.

Bajorek, Agnieszka published the artcileNovel, N-ethyl-2-styrylquinolinum iodides as fluorophores for monitoring of polymerization process, Part I, Synthetic Route of 606-55-3, the publication is Dyes and Pigments (2009), 82(3), 372-378, database is CAplus.

A series of p-substituted 2-styrylquinolinium iodides were prepared by the condensation of N-ethyl-2-methylquinolinium salts with p-substituted benzaldehydes. The spectroscopic properties of the styryl quinolinium dyes are characterized in organic solvents of varying polarities. The electronic absorption and fluorescence emission spectra of the dyes demonstrate their high sensitivity to the nature of substituents introduced into the aromatic ring. The dyes were investigated as fluorescent probes for monitoring the progress of the photochem. initiated free-radical polymerization of a mixture of 2-ethyl-2-(hydroxymethyl)-1,3-propanediol triacrylate and 1-methyl-2-pyrrolidinone. During the course of the polymerization an increase in the fluorescence intensity of the dyes by at least one order of magnitude was recorded; a feature which renders the dyes as good fluorescent probes for such polymerization reactions. The term “probe sensitivity” has been defined and appears in the range from 0.08 to 11 for the styryl dyes.

Dyes and Pigments published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C12H14IN, Synthetic Route of 606-55-3.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Karthigha, S.’s team published research in RSC Advances in 6 | CAS: 606-55-3

RSC Advances published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C12H14IN, Quality Control of 606-55-3.

Karthigha, S. published the artcileSynthesis, growth and third-order nonlinear optical properties of quinolinium single crystal-PCLQI, Quality Control of 606-55-3, the publication is RSC Advances (2016), 6(39), 33159-33169, database is CAplus.

N-Et quinolinium chromophore crystal 2-[2-(4-chloro-phenyl)-vinyl]-1-ethyl-quinolinium iodide (I·I) was successfully grown by the slow evaporation technique. Single crystal X-ray diffraction studies revealed that I·I crystallized in the monoclinic crystal system with the centrosym. space group C2/c. The mol. formation of the grown crystal was initially identified using 1H NMR and FTIR anal. The linear optical studies of crystal I·I were done by UV-vis-NIR studies and thermal studies revealed the stability till its m.p. at 239.7 °C. The grown crystal of I·I exhibited high third order optical nonlinearity which was determined by the Z-scan technique.

RSC Advances published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C12H14IN, Quality Control of 606-55-3.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com

Karthigha, S.’s team published research in Journal of Crystal Growth in 453 | CAS: 606-55-3

Journal of Crystal Growth published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C12H14IN, Category: iodides-buliding-blocks.

Karthigha, S. published the artcileCrystal growth, structural investigation and characterization of newly grown quinolinium derivative single crystal: 1-Ethyl-2-(2-p-tolyl-vinyl)quinolinium; iodide, Category: iodides-buliding-blocks, the publication is Journal of Crystal Growth (2016), 77-89, database is CAplus.

A new N-Et quinolinium derivative of 1-Ethyl-2-(2-p-tolyl-vinyl)-quinoliniumiodide (PTQI) was synthesized by knoevenagel condensation reaction and single crystal was successfully grown by slow evaporation technique. The grown crystal exhibit a centric monoclinic space group P21/C with a third order nonlinear optical response in their crystalline form. The mol. structure of the crystal was studied by single crystal XRD and NMR spectral anal. FTIR reveal the existence of vinyl group and functional groups of the grown crystal. The m.p. and thermal behavior of PTQI were studied using TG/DTA anal. The linear optical study was done by UV-visible-NIR anal. show that the crystal is transparent in the wavelength range of 472-1100 nm. Photoluminescence study shows that PTQI crystal has green luminescence emission property. The etching study reveals that the title crystal encompasses good crystalline nature and lesser amount of dislocations. Third order nonlinear optical property was determined by Z scan technique and the results making grown crystal as a promising material in the field of nonlinear optical devices.

Journal of Crystal Growth published new progress about 606-55-3. 606-55-3 belongs to iodides-buliding-blocks, auxiliary class Quinoline,Salt, name is 1-Ethyl-2-methylquinolin-1-ium iodide, and the molecular formula is C12H14IN, Category: iodides-buliding-blocks.

Referemce:
https://en.wikipedia.org/wiki/Iodide,
Iodide – an overview | ScienceDirect Topics – ScienceDirect.com