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Journal articles on the topic 'Cyclophosphazene'

Author: Grafiati

Published: 4 June 2021

Last updated: 6 September 2023

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1

Yıldırım, Tuba, Elif Şenkuytu, Emel Ergene, Kemal Bilgin, Yıldız Uludağ, and Gönül Yenilmez Çiftçi. "Biological Activity of New Cyclophosphazene Derivatives Including Fluorenylidene-Bridged Cyclophosphazenes." ChemistrySelect 3, no. 34 (2018): 9933–39. http://dx.doi.org/10.1002/slct.201801766.

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2

Chandrasekhar, Vadapalli, Venkatasubbaiah Krishnan, Arunachalampillai Athimoolam, and Gurusamy Thangavelu Senthil Andavan. "New hybrid inorganic-organic polymers containing cyclophosphazenes as pendant groups: Cyclophosphazene ligands containing hydrazone linkages and their conversion to polymers." Canadian Journal of Chemistry 80, no. 11 (2002): 1415–20. http://dx.doi.org/10.1139/v02-099.

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The reaction of the cyclotriphosphazene N3P3Cl5[O-C6H4-p-C6H4-p-CH=CH2] (2) with 10 equiv of N-methylhydrazine proceeds in a regio-specific manner to afford the multi-functional hydrazide N3P3[N(Me)NH2]5[O- C6H4-p-C6H4-p-CH=CH2] (3). Condensation of 3 with o-hydroxy benzaldehyde or pyridine-2-carboxaldehyde affords the corresponding hydrazones N3P3[N(Me)N=CH-C6H4-o-OH]5[O-C6H4-p-C6H4-p-CH=CH2] (4) and N3P3[N(Me)N=CH-C6H4N]5[O-C6H4-p-C6H4-p-CH=CH2] (5), respectively. These hydrazones can be homopolymerized to afford polymers 6 and 7 containing multi-site coordinating cyclophosphazenes as pendan

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3

Po, Riccardo, Luisa Fiocca, Giorgio Giannotta, et al. "Reactive Cyclophosphazenes Containing Oxazoline Groups: the Case of Hexakis(4-Oxazolinophenoxy)Cyclophosphazene." Phosphorus, Sulfur, and Silicon and the Related Elements 168, no. 1 (2001): 269–74. http://dx.doi.org/10.1080/10426500108546566.

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4

Bosscher, G., A. Meetsma, and J. C. van de Grampel. "Novel Organo-Substituted Cyclophosphazenes via Reaction of a Monohydro Cyclophosphazene and Acetyl Chloride." Inorganic Chemistry 35, no. 23 (1996): 6646–50. http://dx.doi.org/10.1021/ic960466b.

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5

Bao, Rui, Jin-Jun Qiu, Shu-Zheng Liu, Tao Cheng, Dong Li, and Cheng-Mei Liu. "Photosensitive Cyclophosphazene and Polyphosphazene." Phosphorus, Sulfur, and Silicon and the Related Elements 183, no. 2-3 (2008): 636–37. http://dx.doi.org/10.1080/10426500701795092.

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6

Allen, Christopher, Robert Hayes, Charles Myer, Amy Freund, and Marie Kearney. "New Organofunctional Cyclophosphazene Derivatives." Phosphorus, Sulfur, and Silicon and the Related Elements 109, no. 1 (1996): 79–82. http://dx.doi.org/10.1080/10426509608545095.

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7

Shimomoto, Hiroaki, Hironori Asano, Tomomichi Itoh, and Eiji Ihara. "Pd-initiated controlled polymerization of diazoacetates with a bulky substituent: synthesis of well-defined homopolymers and block copolymers with narrow molecular weight distribution from cyclophosphazene-containing diazoacetates." Polymer Chemistry 6, no. 26 (2015): 4709–14. http://dx.doi.org/10.1039/c5py00532a.

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8

Po, Riccardo, Luisa Fiocca, Giorgio Giannotta, et al. "ChemInform Abstract: Reactive Cyclophosphazenes Containing Oxazoline Groups: The Case of Hexakis(4-oxazolinophenoxy)cyclophosphazene." ChemInform 33, no. 5 (2010): no. http://dx.doi.org/10.1002/chin.200205265.

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9

Suriya Narayanan, Ramakirushnan, and Vadapalli Chandrasekhar. "Molecular, 1D and 2D assemblies from hexakis(3-pyridyloxy)cyclophosphazene containing 20-membered metallamacrocyclic motifs." Dalton Transactions 45, no. 5 (2016): 2273–83. http://dx.doi.org/10.1039/c5dt03537f.

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10

Uslu, Aylin, and Serkan Yeşilot. "Recent advances in the supramolecular assembly of cyclophosphazene derivatives." Dalton Transactions 50, no. 7 (2021): 2324–41. http://dx.doi.org/10.1039/d0dt04095a.

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11

Krishnadevi, Krishnamoorthy, and Vaithilingam Selvaraj. "Development of halogen-free flame retardant phosphazene and rice husk ash incorporated benzoxazine blended epoxy composites for microelectronic applications." New Journal of Chemistry 39, no. 8 (2015): 6555–67. http://dx.doi.org/10.1039/c5nj00364d.

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12

Kundu, Subrata, Chandrajeet Mohapatra, and Vadapalli Chandrasekhar. "Cyclophosphazene–organostannoxane hybrid motifs in polymeric and molecular systems." RSC Adv. 4, no. 96 (2014): 53662–64. http://dx.doi.org/10.1039/c4ra09371b.

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13

Zuo, Cai, Mengling Yang, Zhijun Wang, et al. "Cyclophosphazene-based hybrid polymer electrolytes obtained via epoxy–amine reaction for high-performance all-solid-state lithium-ion batteries." Journal of Materials Chemistry A 7, no. 32 (2019): 18871–79. http://dx.doi.org/10.1039/c9ta05028k.

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14

Rekha, Pawan, Raeesh Muhammad, and Paritosh Mohanty. "Sonochemical synthesis of cyclophosphazene bridged mesoporous organosilicas and their application in methyl orange, congo red and Cr(vi) removal." RSC Advances 5, no. 83 (2015): 67690–99. http://dx.doi.org/10.1039/c5ra11622h.

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15

Krishnadevi, Krishnamoorthy, Vaithilingam Selvaraj, and Dakshinamoorthy Prasanna. "Thermal, mechanical and antibacterial properties of cyclophosphazene incorporated benzoxazine blended bismaleimide composites." RSC Advances 5, no. 2 (2015): 913–21. http://dx.doi.org/10.1039/c4ra10564h.

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16

Brandt, Krystyna, Teobald Kupka, Jaroslaw Drodz, Johan C. van de Grampel, Auke Meetsma, and Andries P. Jekel. "New dioxytetraethyleneoxy macrocyclic cyclophosphazene derivatives." Inorganica Chimica Acta 228, no. 2 (1995): 187–92. http://dx.doi.org/10.1016/0020-1693(94)04162-o.

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17

Uslu, Aylin, and Serkan Yeşilot. "Chiral configurations in cyclophosphazene chemistry." Coordination Chemistry Reviews 291 (May 2015): 28–67. http://dx.doi.org/10.1016/j.ccr.2015.01.012.

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18

Mutlu Balcı, Ceylan, Süreyya Oğuz Tümay, and Serap Beşli. "ESIPT on/off switching and crystallization-enhanced emission properties of new design phenol-pyrazole modified cyclotriphosphazenes." New Journal of Chemistry 45, no. 19 (2021): 8492–505. http://dx.doi.org/10.1039/d1nj00894c.

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Cyclophosphazene-based high-efficiency excited state intramolecular proton transfer (ESIPT) active and inactive molecules were prepared depending on the different bonding patterns of the difunctional phenol-pyrazol reagent.

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19

Muhammad, Raeesh, Pawan Rekha, and Paritosh Mohanty. "Aminal linked inorganic–organic hybrid nanoporous materials (HNMs) for CO2 capture and H2 storage applications." RSC Advances 6, no. 21 (2016): 17100–17105. http://dx.doi.org/10.1039/c5ra25933a.

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20

Prasanna, Dakshinamoorthy, and Vaithilingam Selvaraj. "Development of non-covalent ternary polymer–CNT composites as a novel supporting material for electrooxidation of glycerol." RSC Advances 5, no. 120 (2015): 98822–33. http://dx.doi.org/10.1039/c5ra17172e.

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A novel ternary polymer–CNT composite containing three different monomers namely amine terminated cyclophosphazene, hexachlorocyclotriphosphazene and 2,2′-benzidinedisulfonic acid as a new catalyst support for biobased alcohol fuel cell applications.

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21

Xia Hu, Ling, Pan He, and Shi jiang Fang. "Study on the Synthesis and Application in the Polycarbonat of Silicone- Cyclophosphazene Flame Retardant." Open Chemical Engineering Journal 9, no. 1 (2015): 29–33. http://dx.doi.org/10.2174/1874123101509010029.

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Silicone-cyclophosphazene (SCP) as a flame retardant was synthesized using hydroxyl terminated polydime thylsiloxane(PDMS-OH) and hexa cyclophosphazene silicone oil and phosphonitrilic chloride trimer(HCCTP) as the precursors, The properties of SCP-modified polycarbonat(PC) such as thermal stability, flame retardant properties and carbon layer after combustion were analyzed. It was found that the target product was SCP, as evidenced by infra-red spectrum (IR)and nuclear magnetic resonance(31P-NMR) spectra results. The PC/SCP composite had higher thermal stability, with higher amount of carbon

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22

Porwolik-Czomperlik, Iwona, Krystyna Brandt, T. Andrew Clayton, David B. Davies, Robert J. Eaton, and Robert A. Shaw. "Diastereoisomeric Singly Bridged Cyclophosphazene-Macrocyclic Compounds." Inorganic Chemistry 41, no. 19 (2002): 4944–51. http://dx.doi.org/10.1021/ic020264h.

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23

Chandrasekhar, Vadapalli, Pakkirisamy Thilagar, and Balasubramanian Murugesa Pandian. "Cyclophosphazene-based multi-site coordination ligands." Coordination Chemistry Reviews 251, no. 9-10 (2007): 1045–74. http://dx.doi.org/10.1016/j.ccr.2006.07.005.

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24

Allcock, Harry R., Karen D. Lavin, and Geoffrey H. Riding. "Ring-opening polymerization of metallocene cyclophosphazene derivatives." Macromolecules 18, no. 6 (1985): 1340–45. http://dx.doi.org/10.1021/ma00148a051.

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25

Chandrasekhar, Vadapalli, Gurusamy Thangavelu Senthil Andavan, Ramachandran Azhakar, and Balasubramanian Murugesa Pandian. "36- and 42-Membered cyclophosphazene-containing macrocycles." Tetrahedron Letters 47, no. 47 (2006): 8365–68. http://dx.doi.org/10.1016/j.tetlet.2006.09.080.

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26

Hagberg, Erik C., Mark W. Hart, Lianhui Cong, Christopher W. Allen, and Kenneth R. Carter. "Cyclophosphazene-containing Polymers as Imprint Lithography Resists." Journal of Inorganic and Organometallic Polymers and Materials 17, no. 2 (2007): 377–85. http://dx.doi.org/10.1007/s10904-007-9130-7.

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27

Inoue, Kenzo, and Tomoyuki Itaya. "Synthesis and Functionality of Cyclophosphazene-Based Polymers." Bulletin of the Chemical Society of Japan 74, no. 8 (2001): 1381–95. http://dx.doi.org/10.1246/bcsj.74.1381.

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28

Sournies, François, François Crasnier, Marcel Graffeuil, et al. "Spherical Cyclophosphazene Dendrimers to the Fifth Generation." Angewandte Chemie International Edition in English 34, no. 5 (1995): 578–81. http://dx.doi.org/10.1002/anie.199505781.

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29

Uslu, Aylin, and Serkan Yesilot. "ChemInform Abstract: Chiral Configurations in Cyclophosphazene Chemistry." ChemInform 46, no. 48 (2015): no. http://dx.doi.org/10.1002/chin.201548244.

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30

Kaur, Tejinder, Tamanna K. Khan, and Mangalampalli Ravikanth. "Multi-Expanded Porphyrin Assemblies on Cyclophosphazene Scaffolds." European Journal of Organic Chemistry 2015, no. 14 (2015): 3157–63. http://dx.doi.org/10.1002/ejoc.201500131.

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31

Kumar, Dheeraj, Jatinder Singh, and Anil J. Elias. "Chiral multidentate oxazoline ligands based on cyclophosphazene cores: synthesis, characterization and complexation studies." Dalton Trans. 43, no. 37 (2014): 13899–912. http://dx.doi.org/10.1039/c4dt01741b.

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Chiral oxazoline derivatives of cyclophosphazenes were prepared and their complexation and catalytic studies for the asymmetric rearrangement of trichloroacetimidates to trichloroacetamides have been performed.

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32

Brandt, Krystyna, Iwona Porwolik, Teobald Kupka, Anna Olejnik, Robert A. Shaw, and David B. Davies. "New Lariat Ether-Type Macrocycles with Cyclophosphazene Subunits." Journal of Organic Chemistry 60, no. 23 (1995): 7433–38. http://dx.doi.org/10.1021/jo00128a014.

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33

DIAZ, C. "Transition metal containing dendrimers based on cyclophosphazene units." Polyhedron 21, no. 9-10 (2002): 909–15. http://dx.doi.org/10.1016/s0277-5387(02)00852-5.

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34

Josowicz, Mira, Jing Li, Charles F. Windisch, et al. "Doping of Poly(cyclophosphazene−benzoquinone) Films with Polyiodide." Chemistry of Materials 9, no. 5 (1997): 1285–91. http://dx.doi.org/10.1021/cm970119f.

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35

Li, Jing, and Mira Josowicz. "Synthesis and Characterization of Electropolymerized Poly(cyclophosphazene−benzoquinone)." Chemistry of Materials 9, no. 6 (1997): 1451–62. http://dx.doi.org/10.1021/cm9701365.

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36

Allcock, Harry R., Eric N. Silverberg, and Gary K. Dudley. "Stereocontrolled Polymerization within a Cyclophosphazene Clathrate Tunnel System." Macromolecules 27, no. 4 (1994): 1033–38. http://dx.doi.org/10.1021/ma00082a023.

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37

Pareek, Yogita, and Mangalampalli Ravikanth. "Multiporphyrin Arrays on Cyclophosphazene Scaffolds: Synthesis and Studies." Chemistry - A European Journal 18, no. 28 (2012): 8835–46. http://dx.doi.org/10.1002/chem.201200273.

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38

Hasselbring, Reinhard, Herbert W. Roesky, Andreas Heine, Dietmar Stalke, and George M. Sheldrick. "Neue Cyclophosphazene mit Metallen der III. Hauptgruppe als Ringbausteine / New Cyclophosphazenes with Metals of Main Group III as Building Blocks." Zeitschrift für Naturforschung B 49, no. 1 (1994): 43–49. http://dx.doi.org/10.1515/znb-1994-0110.

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Abstract Acylic silylated phosphazenes of the type HN(PR2NSiMe3)2 (1) react quantitatively with molecules MMe3 (M = Al, Ga, In) under ring formation and CH4 evolution. The ring compounds N(PPh2NSiMe3)2AlMe2 (2 a) and N(PPh2NSiMe3)2InMe2 (4 a) have been investiga ted by X-ray structure determination. 2a and 4a crystallize in the space groups P 1̄ and P 31, respectively; they show different conformations regarding the cyclohexane framework. NMR spectroscopy of the nuclei in the chelating phosphazene ligand indicates decreasing Lewis acidity of the metal containing fragments in the series AlMe2

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39

Barboiu, Mihai, Cornelia Guran, Ioana Jitaru, Marilena Cimpoesu, and Claudiu T. Supuran. "Complexes With Biologically Active Ligands. Part 71 Synthesis and Fungitoxic Activity of Metal Complexes Containing 1,3,5-tris-(8-Hydroxyquinolino)- Trichlorocyclo-Triphosphazatriene." Metal-Based Drugs 3, no. 5 (1996): 233–40. http://dx.doi.org/10.1155/mbd.1996.233.

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Complexes containing 1,3,5-tris-(8-hydroxyquinolino)-trichlorocyclotriphosphazatriene, a new cyclophosphazene ligand, and Co(II), Cu(II) and Ni(II) were prepared. The new complexes, having the general formula [MLCl2], [ML2]Cl2, (M=Cu, Co, Ni); [NiLAc], [NiL2Ac]Ac and [ML3]X3 (M=Ni, Co, X=Cl, Ac) were characterised by elemental analysis, electronic-, IR spectroscopy, and electrical conductivity measurements. Some of them inhibited the growth of several fungi species (Aspergillus and Candida spp.)

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40

Coles, Simon, David Davies, Michael Hursthouse, Serkan Yeşilot, Bünyemin Çoşut, and Adem Kılıç. "Absolute structure determination as a reference for the enantiomeric resolution of racemic mixtures of cyclophosphazenes via chiral high-performance liquid chromatography." Acta Crystallographica Section B Structural Science 65, no. 3 (2009): 355–62. http://dx.doi.org/10.1107/s0108768109006120.

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Reversed-phase chiral high-performance liquid chromatography (HPLC) is a potentially powerful technique for the enantiomeric resolution of racemic mixtures, although the elution order of enantiomers is only relative and it is necessary to fully characterize reference systems for this method to provide absolute configurational information. The enantiomeric resolution of a series of racemic di-spiro cyclotriphosphazene derivatives, N3P3 X 2[O(CH2)3NH]2 (X = Cl, Ph, SPh, NHPh, OPh) [(1)–(5), respectively] was carried out by reversed-phase chiral HPLC on a commercially available Pirkle-type chiral

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41

Popova, G. V., D. A. Alekperov, T. Sakurai, H. Ihara, and V. V. Kireev. "Synthesis of functional poly(amino acids) on cyclophosphazene templates." Polymer Science Series B 48, no. 4 (2006): 198–202. http://dx.doi.org/10.1134/s1560090406070116.

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42

Furer, V. L., I. I. Vandukova, C. Padie, J. P. Majoral, A. M. Caminade, and V. I. Kovalenko. "FTIR spectroscopy studies of dendrimers built from cyclophosphazene core." Vibrational Spectroscopy 44, no. 1 (2007): 89–93. http://dx.doi.org/10.1016/j.vibspec.2006.09.007.

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43

Paul, Yash, and Sushil K. Pandey. "Synthesis and characterization of cyclophosphazene complexes of zirconium(IV)." Journal of Coordination Chemistry 61, no. 16 (2008): 2655–62. http://dx.doi.org/10.1080/00958970801958527.

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44

Okutan, Elif, Bünyemin Çoşut, and Serkan Yeşilot. "Synthesis and properties of fullerene (C60) substituted cyclophosphazene derivatives." Inorganic Chemistry Communications 49 (November 2014): 1–4. http://dx.doi.org/10.1016/j.inoche.2014.09.006.

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45

Shin, Young Jae, Young Rok Ham, Sun Hee Kim, et al. "Application of cyclophosphazene derivatives as flame retardants for ABS." Journal of Industrial and Engineering Chemistry 16, no. 3 (2010): 364–67. http://dx.doi.org/10.1016/j.jiec.2009.08.001.

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46

Inoue, Kenzo, and Tomoyuki Itaya. "ChemInform Abstract: Synthesis and Functionality of Cyclophosphazene-Based Polymers." ChemInform 32, no. 44 (2010): no. http://dx.doi.org/10.1002/chin.200144255.

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47

Köhler, Jens, Sebastian Kühl, Helmut Keul, Martin Möller, and Andrij Pich. "Synthesis and characterization of polyamine-based cyclophosphazene hybrid microspheres." Journal of Polymer Science Part A: Polymer Chemistry 52, no. 4 (2013): 527–36. http://dx.doi.org/10.1002/pola.27028.

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48

Yenilmez Çiftçi, Gönül. "Synthesis and characterization of per-substituted spermine-bridged cyclophosphazene derivatives: the first example of syn/anti conformational polymorphism in a bridged cyclophosphazene." Inorganic Chemistry Communications 7, no. 12 (2004): 1258–60. http://dx.doi.org/10.1016/j.inoche.2004.09.019.

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49

Poscher, Vanessa, George S. Pappas, Oliver Brüggemann, Ian Teasdale, and Yolanda Salinas. "Hybrid Porous Microparticles Based on a Single Organosilica Cyclophosphazene Precursor." International Journal of Molecular Sciences 21, no. 22 (2020): 8552. http://dx.doi.org/10.3390/ijms21228552.

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Porous organosilica microparticles consisting of silane-derived cyclophosphazene bridges were synthesized by a surfactant-mediated sol-gel process. Starting from the substitution of hexachlorocyclotriphosphazene with allylamine, two different precursors were obtained by anchoring three or six alkoxysilane units, via a thiol-ene photoaddition reaction. In both cases, spherical, microparticles (size average of ca. 1000 nm) with large pores were obtained, confirmed by both, scanning and transmission electron microscopy. Particles synthesized using the partially functionalized precursor containing

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50

Kubono, Koji, Noriko Asaka, Tooru Taga, Seiji Isoda, and Takashi Kobayashi. "Selective clathration in a cage-type host lattice of cyclophosphazene." Journal of Materials Chemistry 4, no. 2 (1994): 291. http://dx.doi.org/10.1039/jm9940400291.

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