Yang, Limin et al. published their research in Spectrochimica Acta, Part A: Molecular and Biomolecular Spectroscopy in 2009 |CAS: 636-73-7

The Article related to frequency vibrational mode homocysteic compound, Optical, Electron, and Mass Spectroscopy and Other Related Properties: Vibrational and Rotational Spectroscopy and other aspects.Safety of Pyridine-3-sulfonic acid

On September 1, 2009, Yang, Limin; Zhao, Guozhong; Li, Weihong; Liu, Yufeng; Shi, Xiaoxi; Jia, Xinfeng; Zhao, Kui; Lu, Xiangyang; Xu, Yizhuang; Xie, Datao; Wu, Jinguang; Chen, Jia’er published an article.Safety of Pyridine-3-sulfonic acid The title of the article was Low-frequency vibrational modes of DL-homocysteic acid and related compounds. And the article contained the following:

Several polycrystalline mols. with sulfonate groups and some of their metal complexes, including DL-homocysteic acid (DLH) and its Sr- and Cu-complexes, pyridine-3-sulfonic acid and its Co- and Ni-complexes, sulfanilic acid and -cysteic acid were studied using THz time-domain methods at room temperature The results of THz absorption spectra show that the mols. have characteristic bands at 0.2-2.7 THz (6-90 cm-1). THz technique can be used to distinguish different mols. with sulfonate groups and to determine the bonding of metal ions and the changes of H bond networks. In the THz region DLH has three bands: 1.61, 1.93 and 2.02 THz; and 0.85, 1.23 and 1.73 THz for Sr-DLH complex, 1.94 THz for Cu-DLH complex, resp. The absorption bands of pyridine-3-sulfonic acid are located at 0.81, 1.66 and 2.34 THz; the bands at 0.96, 1.70 and 2.38 THz for its Co-complex, 0.76, 1.26 and 1.87 THz for its Ni-complex. Sulfanilic acid has three bands: 0.97, 1.46 and 2.05 THz; and the absorption bands of -cysteic acid are at 0.82, 1.62, 1.87 and 2.07 THz, resp. The THz absorption spectra after complexation are different from the ligands, which indicate the bonding of metal ions and the changes of H bond networks. M-O and other vibrations appear in the FIR region for those metal-ligand complexes. The bands in the THz region were assigned to the rocking, torsion, rotation, wagging and other modes of different groups in the mols. Preliminary assignments of the bands were carried out using Gaussian program calculation The experimental process involved the reaction of Pyridine-3-sulfonic acid(cas: 636-73-7).Safety of Pyridine-3-sulfonic acid

The Article related to frequency vibrational mode homocysteic compound, Optical, Electron, and Mass Spectroscopy and Other Related Properties: Vibrational and Rotational Spectroscopy and other aspects.Safety of Pyridine-3-sulfonic acid

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Yamada, Masanori et al. published their research in Chemical Physics Letters in 2005 |CAS: 636-73-7

The Article related to proton conductivity sulfonic phosphonic zwitterionic solid electrolyte fuel cell, Electrochemical, Radiational, and Thermal Energy Technology: Energy-Conversion Devices and Their Components and other aspects.Formula: C5H5NO3S

On February 4, 2005, Yamada, Masanori; Honma, Itaru published an article.Formula: C5H5NO3S The title of the article was Proton conductivity of zwitterionic-type molecular solids under intermediate temperature and anhydrous conditions. And the article contained the following:

Anhydrous proton conducting material for polymer electrolyte membrane fuel cell (PEFC) was prepared by the mixing of zwitterionic-type mol. solid 3-pyridinesulfonic acid (PS) and organic acid methylenediphosphonic acid (MP). As a result, PS mol., which has a sulfonic acid and a pyridine group in its structure, showed the proton conductivity of 4 × 10-5 S cm-1 at 160°C under anhydrous condition. Surprisingly, by the mixing of MP to PS material, the PS-MP composite material exhibited a conductivity of 2 × 10-3 S cm-1. Also, the conductivity of PS-MP composite material did not decrease under the heating at 160° for 50 h. The experimental process involved the reaction of Pyridine-3-sulfonic acid(cas: 636-73-7).Formula: C5H5NO3S

The Article related to proton conductivity sulfonic phosphonic zwitterionic solid electrolyte fuel cell, Electrochemical, Radiational, and Thermal Energy Technology: Energy-Conversion Devices and Their Components and other aspects.Formula: C5H5NO3S

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Liu, Shan-Shan et al. published their research in Inorganic Chemistry in 2020 |CAS: 636-73-7

The Article related to metal organic framework proton conductor porous sulfonic group chromium, Electrochemical, Radiational, and Thermal Energy Technology: Energy-Conversion Devices and Their Components and other aspects.Electric Literature of 636-73-7

On January 6, 2020, Liu, Shan-Shan; Han, Zhen; Yang, Jin-Sen; Huang, Sheng-Zheng; Dong, Xi-Yan; Zang, Shuang-Quan published an article.Electric Literature of 636-73-7 The title of the article was Sulfonic Groups Lined along Channels of Metal-Organic Frameworks (MOFs) for Super-Proton Conductor. And the article contained the following:

Designing high-performance proton-conducting metal-organic frameworks simultaneously having highly hydrothermal stability and a high-d. proton carrier remains a great challenge. Fe-MIL-88B is a classic metal-organic framework (MOF) with a large-size one-dimensional (1D) channel lined with a high-d. uncoordinated metal atom for postfunctionalization; however this MOF cannot act as a proton conductor due to the weak hydrothermal stability. Here, we prepared an ultrastable isostructure Cr-MIL-88B, which is subsequently functionalized by anchoring 3-pyridinesulfonic acid and 2-(4-pyridyl) ethanesulfonic acid on the naked Cr atoms exposed on the surface of the host-framework, producing two new MOFs, i.e. Cr-MIL-88B-pyridine sulfonic acid (abbreviated as Cr-MIL-88B-PSA) and Cr-MIL-88B-pyridine ethanesulfonic acid (abbreviated as Cr-MIL-88B-PESA). Thus, Cr atoms on the host framework were modified by functional sulfonic groups, which stick out toward the center of the channel forming ordered high-d. sulfonic groups as proton donors along the open channel and achieving the highest proton conductivity of 4.50 × 10-2 S cm-1 for Cr-MIL-88B-PESA and 1.58 × 10-1 S cm-1 for Cr-MIL-88B-PSA, surpassing that of the Nafion membrane. The experimental process involved the reaction of Pyridine-3-sulfonic acid(cas: 636-73-7).Electric Literature of 636-73-7

The Article related to metal organic framework proton conductor porous sulfonic group chromium, Electrochemical, Radiational, and Thermal Energy Technology: Energy-Conversion Devices and Their Components and other aspects.Electric Literature of 636-73-7

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Han, Fei et al. published their research in Applied Surface Science in 2018 |CAS: 636-73-7

The Article related to perovskite solar cell self assembled monolayer isomeride passivation, Electrochemical, Radiational, and Thermal Energy Technology: Energy-Conversion Devices and Their Components and other aspects.Reference of Pyridine-3-sulfonic acid

On December 15, 2018, Han, Fei; Tu, Zeyi; Wan, Zhongquan; Luo, Junsheng; Xia, Jianxing; Hao, Guimin; Yi, Yuanping; Wang, Ruilin; Jia, Chunyang published an article.Reference of Pyridine-3-sulfonic acid The title of the article was Effect of functional group position change of pyridinesulfonic acid as interface-modified layer on perovskite solar cell. And the article contained the following:

There are fewer researches on the effect of functional group position change on device performance for highly efficient perovskite solar cell. In this work, we take pyridinesulfonic acid as an example, and study the effect of the isomeride: 2- and 3-pyridinesulfonic acid self-assembled monolayer on device performance for highly efficient perovskite solar cell. The efficiency of control device is 14.65% (Hysteresis Index = 0.31) under illumination of a simulated sunlight (AM 1.5G, 100 mW cm-2). Through use of the 3-pyridinesulfonic acid self-assembled monolayer, the device exhibits striking improvements to reach the efficiency of 16.88% (Hysteresis Index = 0.02), which constitutes an enhancement compared to those of 2-pyridinesulfonic acid self-assembled monolayer modified device (16.54%, Hysteresis Index = 0.02). The enhanced photovoltaic performances can be attributed to the larger perovskite grain sizes, and easier passivation of electron transporting layer/perovskite interface, which promote the charge separation, transport and collection. The experimental process involved the reaction of Pyridine-3-sulfonic acid(cas: 636-73-7).Reference of Pyridine-3-sulfonic acid

The Article related to perovskite solar cell self assembled monolayer isomeride passivation, Electrochemical, Radiational, and Thermal Energy Technology: Energy-Conversion Devices and Their Components and other aspects.Reference of Pyridine-3-sulfonic acid

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Chesnokova, Alexandra N. et al. published their research in Advanced Materials Research (Durnten-Zurich, Switzerland) in 2014 |CAS: 636-73-7

The Article related to polymer electrolyte composite membrane fuel cell property synthesis, Electrochemical, Radiational, and Thermal Energy Technology: Energy-Conversion Devices and Their Components and other aspects.Application of 636-73-7

Chesnokova, Alexandra N.; Lebedeva, Oksana V.; Pozhidaev, Yury N.; Ivanov, Nikolay A.; Rzhechitskii, Alexander E. published an article in 2014, the title of the article was Synthesis and properties of composite membranes for polymer electrolyte membrane fuel cells.Application of 636-73-7 And the article contains the following content:

The paper is devoted to the sol-gel synthesis of proton conductive organic-silicon composite membranes based on tetra-Et orthosilicate (TEOS) and copolymers of 2-methyl-5-vinylpyridine and vinyl chloride (MVP-VC), 2-methyl-5-vinylpyridine and vinyl acetate (MVP-VA), copolymers of ethylene glycol vinyl glycidyl ether and styrene (KS-1 and KS-2), and nitrogen-containing heteroaromatic derivatives of sulfonic acids: 2-phenyl-5-benzimidazolsulfonic acid (PBISA) and pyridine-3-sulfonic acid (PSA). Properties of synthesized membranes, such as proton conductivity, activation energy, ion exchange capacity, dimensional stability have been investigated. The experimental process involved the reaction of Pyridine-3-sulfonic acid(cas: 636-73-7).Application of 636-73-7

The Article related to polymer electrolyte composite membrane fuel cell property synthesis, Electrochemical, Radiational, and Thermal Energy Technology: Energy-Conversion Devices and Their Components and other aspects.Application of 636-73-7

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Yang, Fang-zu et al. published their research in Transactions of the Institute of Metal Finishing in 1998 |CAS: 636-73-7

The Article related to palladium electroplating residual stress, Nonferrous Metals and Alloys: Surface Treatment, Metallic and Nonmetallic Coating, Sealing, Cleaning, Polishing, Etching, and Pickling and other aspects.SDS of cas: 636-73-7

On November 30, 1998, Yang, Fang-zu; Xu, Shu-kai; Huang, Ling; Zhang, Xue-ying; Zhou, Shao-min published an article.SDS of cas: 636-73-7 The title of the article was A study on the effect of bath composition on the internal stress of a palladium electrodeposit. And the article contained the following:

The effects of bath composition on the internal stress of palladium electrodeposits are studied in neutral media with Pd(NH3)2Cl2, K3C6H5O7, (NH4)2C2O4 and the additives of the mixture of the synthesized products of nicotinic acid and nicotiamide (NANA), pyridine-3-sulfonic acid (PSA), α-furan formic acid (FF) and cetyl tri-Me ammonium bromide (CTMAB). The internal stress of electrodeposits is quite changeable at the beginning of electrodeposition, later becoming stable gradually. Deposits obtained from pulse electrodeposition have lower stress than that from d.c. After electrodeposition, all the deposits keep the tensile stress which increases with time. The experimental process involved the reaction of Pyridine-3-sulfonic acid(cas: 636-73-7).SDS of cas: 636-73-7

The Article related to palladium electroplating residual stress, Nonferrous Metals and Alloys: Surface Treatment, Metallic and Nonmetallic Coating, Sealing, Cleaning, Polishing, Etching, and Pickling and other aspects.SDS of cas: 636-73-7

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

McPheat, W. L. et al. published their research in Journal of General Microbiology in 1982 |CAS: 636-73-7

The Article related to nicotinate nicotinamide transport metabolism bordetella, pyridinecarboxaldehyde bordetella nicotinamide uptake inhibition, pyridinealdoxime bordetella nicotinamide uptake inhibition and other aspects.Related Products of 636-73-7

On November 30, 1982, McPheat, W. L.; Wardlaw, A. C. published an article.Related Products of 636-73-7 The title of the article was Inhibition of nicotinic acid and nicotinamide uptake into Bordetella pertussis by structural analogs. And the article contained the following:

The nicotinic acid (I) and nicotinamide (II) structural analogs, 3-pyridinecarboxaldehyde (III) and 3-pyridinealdoxime (IV) (both 500 and 50 μM), but not isonicotinamide, isonicotinic acid, 6-aminonicotinic acid, 6-aminonicotinamide, isoniazid, 3-acetylpyridine, 3-pyridylacetic acid, N,N-diethylnicotinamide, or 3-pyridinesulfonic acid, were effective and specific inhibitors of the uptake of I and II by B. pertussis, although neither compound inhibited the growth of the bacteria in liquid medium or the oxidation of glutamate by washed suspensions. 3-Pyridylcarbinol, at the same dose, was inhibitory, but less so than III and IV. The experimental process involved the reaction of Pyridine-3-sulfonic acid(cas: 636-73-7).Related Products of 636-73-7

The Article related to nicotinate nicotinamide transport metabolism bordetella, pyridinecarboxaldehyde bordetella nicotinamide uptake inhibition, pyridinealdoxime bordetella nicotinamide uptake inhibition and other aspects.Related Products of 636-73-7

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Baker, Paul K. et al. published their research in Journal of the Chemical Society, Dalton Transactions: Inorganic Chemistry in 1995 |CAS: 636-73-7

The Article related to tungsten water soluble seven coordinate complex, pyridinecarboxylate tungsten dinuclear carbonyl complex, pyridinesulfonate pyridinecarboxylate tungsten dinuclear carbonyl complex and other aspects.Application of 636-73-7

On May 7, 1995, Baker, Paul K.; Jenkins, Alyn E.; Lavery, Aidan J.; Muldoon, David J.; Shawcross, Andrew published an article.Application of 636-73-7 The title of the article was The synthesis of the first examples of water-soluble seven-coordinate complexes of tungsten(II). And the article contained the following:

Reaction of the seven-coordinate complex [WI2(CO)3(NCMe)2] with two equivalent of 4-HO2CC5H4N in MeOH at room temperature gave the bis(pyridine-4-carboxylic acid) complex [WI2(CO)3(4-HO2CC5H4N)2] (1) in good yield, which, upon treatment with two equivalent of NaOH in EtOH, afforded the completely water soluble complex [WI2(CO)3(4-NaO2CC5H4N)2] (2) in good yield; reaction of the latter with an equimolar amount of 3-NaO3SC5H4N yielded [WI2(CO)3(4-NaO2CC5H4N)(3-NaO3SC5H4N)], which represents the 1st room-temperature ligand-substitution reaction in H2O of a metal carbonyl complex. The experimental process involved the reaction of Pyridine-3-sulfonic acid(cas: 636-73-7).Application of 636-73-7

The Article related to tungsten water soluble seven coordinate complex, pyridinecarboxylate tungsten dinuclear carbonyl complex, pyridinesulfonate pyridinecarboxylate tungsten dinuclear carbonyl complex and other aspects.Application of 636-73-7

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Funada, Atsushi et al. published their research in Chemistry – An Asian Journal in 2016 |CAS: 636-73-7

The Article related to conformational transformation laurylammonium pyridinesulfonate solid state, conformation analysis, dielectric properties, ionic crystals, liquid crystals, phase transitions and other aspects.Recommanded Product: Pyridine-3-sulfonic acid

Funada, Atsushi; Uchikawa, Shota; Hoshino, Norihisa; Takeda, Takashi; Akutagawa, Tomoyuki published an article in 2016, the title of the article was Conformational Transformations of (C12H25NH3+)(Pyridinesulfonate) in the Solid State.Recommanded Product: Pyridine-3-sulfonic acid And the article contains the following content:

The phase-transition behaviors, crystal structures, and dielec. properties of four kinds of simple 1:1 organic salts of (C12H25NH3+)(benzenesulfonate) and (C12H25NH3+)(pyridine sulfonates) were examined from the viewpoint of intermol. hydrogen-bonding interactions and dynamic conformational transformation in mol. assemblies. Crystals of (C12H25NH3+)(benzenesulfonate) and (C12H25NH3+)(3-pyridinesulfonate) were isostructural and solid-solid and solid-liquid-crystal smectic A (SmA) phase transitions were observed These two crystals formed rodlike cation-anion assemblies. However, the two salts, (C12H25NH3+)(2-pyridinesulfonate) and (C12H25NH3+)(4-pyridinesulfonate), formed largely bent L-shaped cation-anion conformations. Interesting conformational transformations from rodlike to L-shaped assemblies were observed in (C12H25NH3+)(2-pyridinesulfonate) and (C12H25NH3+)(3-pyridinesulfonate). The experimental process involved the reaction of Pyridine-3-sulfonic acid(cas: 636-73-7).Recommanded Product: Pyridine-3-sulfonic acid

The Article related to conformational transformation laurylammonium pyridinesulfonate solid state, conformation analysis, dielectric properties, ionic crystals, liquid crystals, phase transitions and other aspects.Recommanded Product: Pyridine-3-sulfonic acid

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem

Varghese, Hema Tresa et al. published their research in Asian Journal of Chemistry in 2007 |CAS: 636-73-7

The Article related to pyridinesulfonic acid vibrational spectroscopy ab initio, Physical Organic Chemistry: Absorption, Emission, Reflection, and Scattering Spectra (Ultraviolet and Visible, Infrared and Fourier Transform Infrared, Raman, Microwave, Photoelectron, Fluorescence, Phosphorescence, etc.) and other aspects.Category: pyridine-derivatives

On August 31, 2007, Varghese, Hema Tresa; Panicker, C. Yohannan; Anto, P. L.; Philip, Daizy published an article.Category: pyridine-derivatives The title of the article was Vibrational spectroscopic studies and ab initio calculations of pyridine-3-sulfonic acid. And the article contained the following:

FT-Raman and FT-IR spectra of pyridine-3-sulfonic acid were recorded and analyzed. The mol. geometry and vibrational wave numbers of pyridine-3-sulfonic acid have been calculated using the Hartree-Fock method with different basis sets. Comparison of the observed fundamental vibrational wavenumbers of pyridine-3-sulfonic acid with calculated results by Hartree-Fock method is found in agreement with the exptl. data. The experimental process involved the reaction of Pyridine-3-sulfonic acid(cas: 636-73-7).Category: pyridine-derivatives

The Article related to pyridinesulfonic acid vibrational spectroscopy ab initio, Physical Organic Chemistry: Absorption, Emission, Reflection, and Scattering Spectra (Ultraviolet and Visible, Infrared and Fourier Transform Infrared, Raman, Microwave, Photoelectron, Fluorescence, Phosphorescence, etc.) and other aspects.Category: pyridine-derivatives

Referemce:
Pyridine – Wikipedia,
Pyridine | C5H5N – PubChem