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Relevant bibliographies by topics / Polymers Pyridine Carboxylic acids

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Academic literature on the topic 'Polymers Pyridine Carboxylic acids'

Author: Grafiati

Published: 4 June 2021

Last updated: 6 February 2022

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Journal articles on the topic "Polymers Pyridine Carboxylic acids"

1

Zhang, Xiu-Du, Ji-Ai Hua, Jin-Han Guo, Yue Zhao, and Wei-Yin Sun. "Cadmium(ii) coordination polymers based on 2-(4-((E)-2-(pyridine-2-yl)vinyl)styryl)pyridine and dicarboxylate ligands as fluorescent sensors for TNP." Journal of Materials Chemistry C 6, no. 46 (2018): 12623–30. http://dx.doi.org/10.1039/c8tc04557g.

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Three novel coordination polymers have been synthesized based on Cd(ii) and 2-(4-((E)-2-(pyridine-2-yl)vinyl)styryl)pyridine by employing different carboxylic acids as auxiliary ligands. All of them can function as fluorescent sensors for TNP with high sensitivity, selectivity and recyclability.

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Gu, Jinzhong, Min Wen, Xiaoxiao Liang, Zifa Shi, Marina Kirillova, and Alexander Kirillov. "Multifunctional Aromatic Carboxylic Acids as Versatile Building Blocks for Hydrothermal Design of Coordination Polymers." Crystals 8, no. 2 (2018): 83. http://dx.doi.org/10.3390/cryst8020083.

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Selected recent examples of coordination polymers (CPs) or metal-organic frameworks (MOFs) constructed from different multifunctional carboxylic acids with phenyl-pyridine or biphenyl cores have been discussed. Despite being still little explored in crystal engineering research, such types of semi-rigid, thermally stable, multifunctional and versatile carboxylic acid building blocks have become very promising toward the hydrothermal synthesis of metal-organic architectures possessing distinct structural features, topologies, and functional properties. Thus, the main aim of this mini-review has

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3

Guo, Yuanyuan, Pengtao Ma, Jingping Wang, and Jingyang Niu. "Two multi-dimensional frameworks constructed from zinc coordination polymers with pyridine carboxylic acids." Journal of Solid State Chemistry 184, no. 11 (2011): 3121–27. http://dx.doi.org/10.1016/j.jssc.2011.09.030.

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4

Smith, Graham, Katherine E. Baldry, Karl A. Byriel, and Colin H. L. Kennard. "Molecular Cocrystals of Carboxylic Acids. XXV The Utility of Urea in Structure Making with Carboxylic Acids and the Crystal Structures of a Set of Six Adducts with Aromatic Acids." Australian Journal of Chemistry 50, no. 7 (1997): 727. http://dx.doi.org/10.1071/c96199.

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Molecular adducts of urea with six aromatic carboxylic acids have been prepared and characterized by using X-ray diffraction methods and infrared spectroscopy. These compounds are with 5-nitrosalicylic acid [(C7H5NO5)2(CH4N2O)] (1), 3,5-dinitrosalicylic acid [(C7H4N2O7)(CH4N2O)] (2), 4-aminobenzoic acid [(C7H7NO2)2(CH4N2O)] (3), o-phthalic acid [(C8H6O4)(CH4N2O)] (4), pyrazine-2,3-dicarboxylic acid [(C4H4N2O4)(CH4N2O)] (5) and pyridine-2,6-dicarboxylic acid [(C7H5NO4)(CH4N2O)2] (6). In the majority of the adducts, all six potential interactive sites on the urea molecules are utilized in hydrog

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5

Toma, Monica, Agustín Sánchez, José Casas, et al. "New thallium(III) chloride complexes with pyridine carboxylic acids: from molecular compounds to supramolecular associations." Open Chemistry 1, no. 4 (2003): 441–64. http://dx.doi.org/10.2478/bf02475227.

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AbstractReactions of TlCl3 with picolinic acid (Hpic), nicotinic acid (Hnic), isonicotinic acid (Hinic) and 3-hydroxy-picolinic acid (H3hpic) afford the isolation of new chlorothallium(III) complexes. The compounds are characterized by IR, Raman and multinuclear NMR (1H,13C,205Tl). The molecular structures of [TlCl2(pic)(Hpic)]·0.5H2O (1), [TlCl2(nic)(Hnic)] (2), [TlCl(inic)2]·0.6C2H5OH (3) and [TlCl(3hpic)2(h3hpic)] (4) are determined by single-crystal X-ray diffraction. A distorted octahedral TlCl2N2O2 core containing the O,N-chelating ligands is achieved in the monomeric complex 1. The coor

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6

Faghihi, Khalil, Mostafa Ashouri, and Mohsen Hajibeygi. "High Temperature and Organosoluble Poly(amide-imide)s Based on 1,4-Bis[4-aminophenoxy]butane and Aromatic Diacids by Direct Polycondensation: Synthesis and Properties." High Temperature Materials and Processes 32, no. 5 (2013): 451–58. http://dx.doi.org/10.1515/htmp-2012-0164.

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AbstractA series of high temperature and organosoluble poly(amide-imide)s 8a–g were prepared by direct polycondensation from 1,4-bis[4-aminophenoxy]butane 4 and various aromatic diacids 7a–g in a medium consisting of N-methyl-2-pyrrolidone (NMP)/triphenyl phosphite (TPP)/calcium chloride (CaCl2)/pyridine system. Aromatic diacids 7a–g were synthesized by reaction of 3,3′,4,4′-benzophenone tetra carboxylic dianhydride 5 and various amino acids 6a–g. All of the above polymers were fully characterized by 1H-NMR and FT-IR spectroscopy, inherent viscosity, solubility test and thermogravimetric analy

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7

Gu, Jinzhong, Min Wen, Yan Cai, et al. "Cobalt(II) Coordination Polymers Assembled from Unexplored Pyridine-Carboxylic Acids: Structural Diversity and Catalytic Oxidation of Alcohols." Inorganic Chemistry 58, no. 9 (2019): 5875–85. http://dx.doi.org/10.1021/acs.inorgchem.9b00242.

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8

Ostapova, Elena V., Sergey Yu Lyrschikov, and Heinrich N. Altshuler. "Equilibrium constants of the sorption of pyridinecarboxylic acids by polystyrene type sulfocationite." Butlerov Communications 64, no. 10 (2020): 55–62. http://dx.doi.org/10.37952/roi-jbc-01/20-64-10-55.

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The processes of sorption of pyridine-3-carboxylic (nicotinic) and pyridine-4-carboxylic (isonicotinic) acids by sulfonic acid cation exchangers of the polystyrene type (CU-2-4 and CU-2-8) from aqueous solutions with different pH values were studied. Analysis of the FTIR spectra of isonicotinic acid, isonicotinic acid sulfate, and CU-2-8 sulfonic cation exchanger filled with isonicotinic acid showed that pyridinecarboxylic acid is in the protonated form in the polymer phase. Experimental data of the equilibrium distribution of acids in the aqueous solution-cation exchange system have been obta

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Ruaa Jameel Kamel, Mohammed Ali Mutar, and Farah Safi Khlewee. "Synthesis and characterization of new diacid monomers and poly (ester-imide) s: a study of thermal property relationship and solubility." International Journal of Research in Pharmaceutical Sciences 10, no. 3 (2019): 1936–41. http://dx.doi.org/10.26452/ijrps.v10i3.1397.

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Two dicarboxylic acids [2,2'-(((4-hydroxyphenyl) methylene) bis (3-Bromo-4,1- phenylene)) bis (1,3 dioxoisoindoline 5 carboxylic acid)) and 2,2 '(((2,4dichlorophenyl) methylene) bis (4,1-phenylene)) bis (1,3-dioxoisoindoline-5-carboxylic acid)] were made by the reaction of pyromellitic anhydride (PMDA) with diamine in a solvent of g pyridine/glacial acetic acid at refluxing temperature. The organization of the diacid monomers is defined by FTIR and 1H-NMR spectroscopy. The sequence of new poly (ester-imide) s are arranged of two di acids and aromatic diols: [Bis (4hydroxyphenyl) 2 furelmethane

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Ju, Hai-Yan, Gang Zhang, Ming Yang, De-Zheng Liu, Yong-Sheng Yang, and Yan-Bo Zhang. "Synthesis, Crystal Structures and Luminescence Properties of Three New Cadmium 3D Coordination Polymers." Molecules 25, no. 11 (2020): 2465. http://dx.doi.org/10.3390/molecules25112465.

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The new rigid planar ligand 2,5-bis(3-(pyridine-4-yl)phenyl)thiazolo[5,4-d]thiazole (BPPT) has been synthesized, which is an excellent building block for assembling coordination polymer. Under solvothermal reaction conditions, cadmium ion with BPPT in the presence of various carboxylic acids including (1,1′-biphenyl)-4,4′-dicarboxylic acid (BPDC), isophthalic acid (IP), and benzene-1,3,5-tricarboxylic acid (BTC) gave rise to three coordination complexes, viz, [Cd(BPPT)(BPDA)](BPPT)n (1), [Cd(BPPT) (IP)] (CH3OH) (2), and [Cd3(BPPT)3(BTC)2(H2O)2] (3). The structures of 1, 2, and 3 were character

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Dissertations / Theses on the topic "Polymers Pyridine Carboxylic acids"

1

Yu, Sze-chit. "Syntheses and physical properties of polymers based on 2,2'-bipyridine dicarboxylic acid and pyridine-2,6-dicarboxylic acid /." Hong Kong : University of Hong Kong, 1999. http://sunzi.lib.hku.hk/hkuto/record.jsp?B20978650.

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余思捷 and Sze-chit Yu. "Syntheses and physical properties of polymers based on 2,2'-bipyridinedicarboxylic acid and pyridine-2,6-dicarboxylic acid." Thesis, The University of Hong Kong (Pokfulam, Hong Kong), 1999. http://hub.hku.hk/bib/B31239705.

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Lee, Chien-Ming. "Hydrogen-bonded main-chain liquid crystalline association polymers." Thesis, University of Cambridge, 1994. https://www.repository.cam.ac.uk/handle/1810/272680.

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4

Tse, Hiu Wah. "Hydrothermal synthesis of metal carboxylate polymers using high coordination number metals /." View abstract or full-text, 2004. http://library.ust.hk/cgi/db/thesis.pl?CHEM%202004%20TSE.

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Disch, Jeremy S. "Di- and tetratopic pyridine appended cyclidenes as "molecular tweezers" : structure and carboxylic acid NMR binding studies /." Thesis, Connect to Dissertations & Theses @ Tufts University, 2004.

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Thesis (Ph.D.)--Tufts University, 2004.<br>Adviser: Elena V. Rybak-Akimova. Submitted to the Dept. of Chemistry. Includes bibliographical references (leaves 381-387). Access restricted to members of the Tufts University community. Also available via the World Wide Web;

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Sanchez-Ballester, Noelia M. "Supramolecular studies with functionalised group 15 ligands." Thesis, Loughborough University, 2010. https://dspace.lboro.ac.uk/2134/6062.

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This thesis has been divided into five sections. The first chapter introduces the main themes of this thesis, including the description of the concepts of supramolecular chemistry, crystal engineering, hydrogen bonding and graph set analysis. The final section of chapter one describes a typical X-ray experiment used to determine the structures of the compounds presented in this thesis. Chapter two describes the synthesis and single crystal structures of copper(I) complexes with pyridine- and pyrazine-carboxylic acids. A series of novel solvent inclusion compounds of copper(I) complexes with py

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7

Beaman, Daniel Keith 1978. "Vibrational sum-frequency spectroscopy investigations of carboxylic acid based surfactants and polymers at the oil-water interface." Thesis, University of Oregon, 2010. http://hdl.handle.net/1794/11148.

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xv, 116 p. : ill. A print copy of this thesis is available through the UO Libraries. Search the library catalog for the location and call number.<br>Aqueous solutes next to hydrophobic interfaces arc prevalent in a multitude of chemical and biological systems throughout the world. Their presence ranges from environmental processes such as soil and water remediation to biological processes such as ion transport, membrane formation, and enzyme activity. In these and other examples, the interface is an integral part of the system. Understanding these chemically complex systems requires that a m

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8

Al-Sousi, Ghareeb N. "Studies on the thermal decomposition behaviour, kinetics and electrical conductivity of the non-isothermal decomposition of pyridine mono carboxylic acids and some of their transition metal complexes." Thesis, Aston University, 2000. http://publications.aston.ac.uk/9623/.

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The thesis is divided into four chapters. They are: introduction, experimental, results and discussion about the free ligands and results and discussion about the complexes. The First Chapter, the introductory chapter, is a general introduction to the study of solid state reactions. The Second Chapter is devoted to the materials and experimental methods that have been used for carrying out the experiments. The Third Chapter is concerned with the characterisations of free ligands (Picolinic acid, nicotinic acid, and isonicotinic acid) by using elemental analysis, IR spectra, X-ray diffraction,

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9

NASCIMENTO, CARLOS E. "Síntese de superabsorventes poliméricos biodegradáveis por meio da extrusão reativa do Poli (álcool vinílico) e amido, em presença de aldeído e ácido glioxílico, para uso agrícola." reponame:Repositório Institucional do IPEN, 2016. http://repositorio.ipen.br:8080/xmlui/handle/123456789/26937.

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Submitted by Marco Antonio Oliveira da Silva (maosilva@ipen.br) on 2016-12-21T18:14:50Z No. of bitstreams: 0<br>Made available in DSpace on 2016-12-21T18:14:50Z (GMT). No. of bitstreams: 0<br>Com a alta taxa de desertificação dos solos e a necessidade de irrigação constante dos plantios, existe a necessidade da criação de um polímero superabsorvente (SAP) com a característica de ser biodegradável. Observando o estágio tecnológico relacionado às atividades de pesquisa e desenvolvimento de SAPs no Brasil, foi utilizado o poli (álcool vinílico)/PVA e o amido de mandioca para a formação de hidrog

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10

Yen, Chia-Hung, and 嚴佳宏. "A Study on Hydrothermal Synthesis and Structures of Transition-Metal Coordination Polymers of Pyridine-carboxylic and -dicarboxylic Acid." Thesis, 2004. http://ndltd.ncl.edu.tw/handle/29370135531577774153.

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碩士<br>國立成功大學<br>化學系碩博士班<br>93<br>Transition-Metal compounds of CoCl2 , Zn(NO3)2, Pb(NO3)2, Ni(OAc)2, and Ni(NO3)2 reacted hydrothermally with pyridyl mono- or dicarboxylic acid of 3-pcH, 4-pcH, 2,3-pdcH2, 2,4-pdcH2, 2,5-pdcH2, 2,6-pdcH2, 3,4-pdcH2, and 3,5-pdcH2 in a autogenous stainless steel bomb under 110-190℃ to produce 0-, 1-, 2-, and 3-dimensional (0D, 1D, 2D, 3D) structures within 10-72 hours (3-pcH=3-pyridylcarboxylic acid, 4-pcH=4-pyridylcarboxylic acid, 2,3-pdcH2=pyridine-2,3-dicarboxylic acid, 2,4-pdcH2=pyridine-2,4-dicarboxylic acid, 2,5-pdcH2=pyridine-2,5-dicarboxylic ac

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Books on the topic "Polymers Pyridine Carboxylic acids"

1

Holder, Alvin A. Dipicolinic acid, its analogues and derivatives: Aspects of their coordination chemistry. Nova Science Publishers, 2011.

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2

Piemonte, Vincenzo. Polylactic acid: Synthesis, properties, and applications. Nova Science Publishers, 2011.

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Piemonte, Vincenzo. Polylactic Acid: Synthesis, Properties and Applications. Nova Science Publishers, Incorporated, 2014.

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Ruseckaite, Roxana, Alejandro Muller, Iiaria Armentano, Mercedes Peltzer, and Mercedes Peltzer. Poly Science and Technology: Processing, Properties, Additives and Applications. Royal Society of Chemistry, The, 2014.

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Book chapters on the topic "Polymers Pyridine Carboxylic acids"

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Godfrey, John C. "Pyridine Side-Chain Carboxylic Acids." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186671.ch3.

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Neubert, Mary E. "Pyridine Side-Chain Carboxylic Acids." In Chemistry of Heterocyclic Compounds: A Series Of Monographs. John Wiley & Sons, Inc., 2008. http://dx.doi.org/10.1002/9780470186725.ch4.

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Jong, Lei, and John C. Saam. "Polycondensation of Carboxylic Acids and Carbinols in Heterogeneous Media." In Step-Growth Polymers for High-Performance Materials. American Chemical Society, 1996. http://dx.doi.org/10.1021/bk-1996-0624.ch021.

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Keller, P. A. "Activation of Acid Chlorides Using Pyridine-2-thiones." In Three Carbon-Heteroatom Bonds: Acid Halides; Carboxylic Acids and Acid Salts. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-020-00626.

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Sáenz-Galindo, Aidé, Lluvia I. López-López, Fabiola N. de la Cruz-Duran, et al. "Applications of Carboxylic Acids in Organic Synthesis, Nanotechnology and Polymers." In Carboxylic Acid - Key Role in Life Sciences. InTech, 2018. http://dx.doi.org/10.5772/intechopen.74654.

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Wu, Y. J. "Cyclization of 3-Nitrogen-Functionalized Pyridine-4-carboxylic Acids with Nitrogen-Containing Compounds." In Six-Membered Hetarenes with Two Identical Heteroatoms. Georg Thieme Verlag KG, 2012. http://dx.doi.org/10.1055/sos-sd-116-00670.

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Nelson, S. G. "Reactions of Carboxylate Esters and Anhydrides with Hydrogen Fluoride or Hydrogen Fluoride/Pyridine." In Three Carbon-Heteroatom Bonds: Acid Halides; Carboxylic Acids and Acid Salts. Georg Thieme Verlag KG, 2007. http://dx.doi.org/10.1055/sos-sd-020-00012.

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Olah, George A., Masatomo Nojima, and Istvan Kerekes. "Synthetic Methods and Reactions. I: Selenium Tetrafluoride and Its Pyridine Complex. Convenient Fluorinating Agents for Fluorination of Ketones, Aldehydes, Amides, Alcohols, Carboxylic Acids, and Anhydrides." In World Scientific Series in 20th Century Chemistry. World Scientific Publishing Company, 2003. http://dx.doi.org/10.1142/9789812791405_0203.

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Dalton, David R. "The Leaf." In The Chemistry of Wine. Oxford University Press, 2018. http://dx.doi.org/10.1093/oso/9780190687199.003.0016.

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Grape leaves are thin and flat. As is common among leaves in general, they are composed of different sets of specialized cells. Today, on average, sunlight reaching their surface is about 4% ultraviolet (UV) (<400 nm), 52% infrared (IR) (>750 nm) and 44% visible (VIS) radiation. Little of the UV and IR are used by plants. As with other leaves that are green, only the red and blue ends of the visible part of the electromagnetic spectrum are absorbed, thus leaving green available by reflection and transmission. On the surface of the leaf (Figure 8.1), the cells of the outermost layer (the epidermis) are designed to protect the inner cells where the workings needed for gathering the sunlight used for photosynthesis and other chemistry necessary to the life of the plant are found. That is, the more delicate cells, beneath the epidermis, are involved in production of carbohydrates as well as the movement of nutrients in and products out of the leaf. The epidermis, exposed to the atmosphere, has cells that are usually thicker and are covered by a waxy layer made up of long- chain carboxylic acids that have hydroxyl groups (–OH) at or near their termini. These so-called omega hydroxy acids can then form esters using the hydroxyl group of one and the carboxylic acid of the next. This yields long-chain polyester polymers called “cutin.” As indicated in the earlier discussion of cells and, in particular, regarding the fatty acids of cell walls, the fatty acids found in the epidermis generally consist of an even number of carbon atoms, and for cutin, the sixteen carbon (palmitic acid) family (Figure 8.2) and the eighteen carbon family (oleic acid bearing a double bond or the saturated analogue stearic acid) are common. While one terminal hydroxyl group is usual (e.g., 16-hydroxypalmitic acid, 18-hydroxyoleic acid, or its saturated analogue 18-hydroxystearic acid) more than one (allowing for cross-linking) is not uncommon (e.g., 10,16-dihydroxypalmitic and 9,10,18-trihydroxystearic acid).

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Taber, Douglass F. "Heteroaromatics: The Mal Synthesis of Clausevatine D." In Organic Synthesis. Oxford University Press, 2013. http://dx.doi.org/10.1093/oso/9780199965724.003.0066.

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Huanfeng Jiang of the South China University of Technology showed (J. Org. Chem. 2010, 75, 966) that an alkynoate 1 could be condensed with a 1,3-dicarbonyl compound 2 to give, under oxidizing conditions, the furan 3. Phil Ho Lee of Kangwon National University found (Tetrahedron Lett. 2010, 51, 1899) that the enyne 4 cyclized smoothly to the furan 5. Yahong Li of Suzhou University and Vladimir Gevorgyan of the University of Illinois, Chicago, demonstrated (J. Am. Chem. Soc. 2010, 132, 7645) that the cyclization of 6 proceeded with silyl migration, to give 7. François Bilodeau and Pat Forgione of Boehringer Ingelheim (Canada) optimized (J. Org. Chem. 2010, 75, 1550) the Pd-mediated decarboxylative coupling of a furoic acid 8 with 9 to give 10. This protocol also worked well with pyrrole carboxylic acids. In another transformation of a preformed pyrrole, Masatomo Iwao of Nagasaki University observed (Organic Lett. 2010, 12, 2734) that in the presence of LDA/diisopropylamine, the initially formed 2-anion from the deprotonation of 11 gave the 2-product 12 with more reactive electrophiles but the 5-product 13 with less reactive electrophiles. Umasish Jana of Jadavpur University developed (J. Org. Chem. 2010, 75, 1674) a route to more highly substituted pyrroles such as 17 using the remarkable four-component coupling of 14, 15, and 16 with nitromethane, the carbon of which was incorporated in the product. Laura L. Anderson, also of the University of Illinois, Chicago, designed (Organic Lett. 2010, 12, 2290) a clever approach to pyrroles, based on the Ir-catalyzed rearrangement of O-allyl oximes such as 18. Xiaofeng Tong of the East China University of Science and Technology reported (Chem. Commun. 2010, 312) the condensation of 20 with 21 to give the dihydropyridine 22. Base-mediated elimination of sulfinate could convert 22 into the pyridine. Jin-Quan Yu of Scripps/La Jolla found (Angew. Chem. Int. Ed. 2010, 49, 1275) that Pd-mediated activation of the nictotinamide 23 proceeded with high regioselectivity, leading to 25. Zhiping Li of Remnin University of China demonstrated (J. Org. Chem. 2010, 75, 4636) that the chloroenamine 26 cyclized to the indole 27 on exposure to NaI.

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Reports on the topic "Polymers Pyridine Carboxylic acids"

1

Fife, Wilmer K., and Martel Zeldin. Structural Synergism in Functionalized Polymers: New Catalysts for Transacylation Reactions of Derivatives of Carboxylic and Phosphoric Acids. Defense Technical Information Center, 1991. http://dx.doi.org/10.21236/ada236921.

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