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Journal articles on the topic 'Poly(propylene imine)-co-polypyrrole'

Author: Grafiati

Published: 4 June 2021

Last updated: 2 February 2022

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1

Baleg, Abd Almonam, Nazeem Jahed, Anne L. Djoumessi Yonkeu, et al. "Impedimetry and microscopy of electrosynthetic poly(propylene imine)-co-polypyrrole conducting dendrimeric star copolymers." Electrochimica Acta 128 (May 2014): 448–57. http://dx.doi.org/10.1016/j.electacta.2013.12.138.

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2

Baleg, Abd Almonam A., Nazeem M. Jahed, Omotayo A. Arotiba, et al. "Synthesis and characterization of poly(propylene imine) dendrimer – Polypyrrole conducting star copolymer." Journal of Electroanalytical Chemistry 652, no. 1-2 (2011): 18–25. http://dx.doi.org/10.1016/j.jelechem.2010.12.010.

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3

Froehling, Peter, and Josephine Brackman. "Properties and applications of poly(propylene imine) dendrimers and poly(esteramide) hyperbranched polymers." Macromolecular Symposia 151, no. 1 (2000): 581–89. http://dx.doi.org/10.1002/1521-3900(200002)151:1<581::aid-masy581>3.0.co;2-t.

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4

Ntshongontshi, Nomaphelo, Abd Almonam A. Baleg, Rachel Fanelwa Ajayi, et al. "Cytochrome P450-3A4/Copper-Poly(Propylene Imine)-Polypyrrole Star Co-Polymer Nanobiosensor System for Delavirdine - A Non-Nucleoside Reverse Transcriptase Inhibitor HIV Drug." Journal of Nano Research 44 (November 2016): 265–80. http://dx.doi.org/10.4028/www.scientific.net/jnanor.44.265.

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HIV and AIDS are among the world’s pandemics that pose serious concern to almost every individual in the world. With the current level of availability of anti-retroviral (ARV) drugs and the ease of accessibility of treatment in many countries such as South Africa, the disease can be controlled by suppressing the viral load of an infected individual. These anti HIV drugs such as delavirdine are metabolised by enzymes which are found in the liver microsomes, particularly those of the cytochrome P450 family. Due to the fact that the metabolic rate of a patient determines the effect of the drug, t

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5

Felczak, Aleksandra, Katarzyna Zawadzka, Natalia Wrońska, et al. "Enhancement of antimicrobial activity by co-administration of poly(propylene imine) dendrimers and nadifloxacin." New Journal of Chemistry 37, no. 12 (2013): 4156. http://dx.doi.org/10.1039/c3nj00760j.

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6

Wrońska, N., A. Felczak, K. Zawadzka, et al. "The antibacterial effect of the co-administration of poly(propylene imine) dendrimers and ciprofloxacin." New Journal of Chemistry 38, no. 7 (2014): 2987. http://dx.doi.org/10.1039/c3nj01338c.

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7

Kabanov, V. A. "Polyelectrolyte behavior and interpolyelectrolyte matching of AstramolTM poly(propylene imine) dendrimers." Macromolecular Symposia 175, no. 1 (2001): 265–72. http://dx.doi.org/10.1002/1521-3900(200110)175:1<265::aid-masy265>3.0.co;2-l.

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8

Kreider, Jason L., and Warren T. Ford. "Quaternary ammonium ion dendrimers from methylation of poly(propylene imine)s." Journal of Polymer Science Part A: Polymer Chemistry 39, no. 6 (2001): 821–32. http://dx.doi.org/10.1002/1099-0518(20010315)39:6<821::aid-pola1055>3.0.co;2-f.

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9

Takada, Kazutake, Diego J. Díaz, Héctor D. Abruña, et al. "Cobaltocenium-Functionalized Poly(propylene imine) Dendrimers: Redox and Electromicrogravimetric Studies and AFM Imaging." Chemistry 7, no. 5 (2001): 1109–17. http://dx.doi.org/10.1002/1521-3765(20010302)7:5<1109::aid-chem1109>3.0.co;2-#.

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10

Baars, Maurice W. P. L., Ralf Kleppinger, Michel H. J. Koch, Siang-Lie Yeu, and E. W. Meijer. "The Localization of Guests in Water-Soluble Oligoethyleneoxy-Modified Poly(propylene imine) Dendrimers." Angewandte Chemie International Edition 39, no. 7 (2000): 1285–88. http://dx.doi.org/10.1002/(sici)1521-3773(20000403)39:7<1285::aid-anie1285>3.0.co;2-f.

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11

Baars, Maurice W P. L., Ralf Kleppinger, Michel H J. Koch, Siang-Lie Yeu, and E. W. Meijer. "The Localization of Guests in Water-Soluble Oligoethyleneoxy-Modified Poly(propylene imine) Dendrimers." Angewandte Chemie 112, no. 7 (2000): 1341–44. http://dx.doi.org/10.1002/(sici)1521-3757(20000403)112:7<1341::aid-ange1341>3.0.co;2-q.

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12

I. Peerlings, H. W., Sergey A. Nepogodiev, J. Fraser Stoddart, and E. W. Meĳer. "Synthesis of Spacer-Armed Glucodendrimers Based on the Modification of Poly(propylene Imine) Dendrimers." European Journal of Organic Chemistry 1998, no. 9 (1998): 1879–86. http://dx.doi.org/10.1002/(sici)1099-0690(199809)1998:9<1879::aid-ejoc1879>3.0.co;2-8.

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13

Baars, Maurice W. P. L., Serge H. M. Söntjens, Hartmut M. Fischer, H. W. I. Peerlings, and E. W. Meijer. "Liquid-Crystalline Properties of Poly(propylene imine) Dendrimers Functionalized with Cyanobiphenyl Mesogens at the Periphery." Chemistry - A European Journal 4, no. 12 (1998): 2456–66. http://dx.doi.org/10.1002/(sici)1521-3765(19981204)4:12<2456::aid-chem2456>3.0.co;2-l.

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14

Mazzaracchio, Vincenzo, Luthando Tshwenya, Danila Moscone, Fabiana Arduini, and Omotayo A. Arotiba. "A Poly(Propylene Imine) Dendrimer and Carbon Black Modified Flexible Screen Printed Electrochemical Sensor for Lead and Cadmium Co‐detection." Electroanalysis 32, no. 12 (2020): 3009–16. http://dx.doi.org/10.1002/elan.202060284.

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15

Vassilev, Krassimir, and Warren T. Ford. "Poly(propylene imine) dendrimer complexes of Cu(II), Zn(II), and Co(III) as catalysts of hydrolysis ofp-nitrophenyl diphenyl phosphate." Journal of Polymer Science Part A: Polymer Chemistry 37, no. 15 (1999): 2727–36. http://dx.doi.org/10.1002/(sici)1099-0518(19990801)37:15<2727::aid-pola6>3.0.co;2-s.

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16

Vassilev, Krassimir, Jason Kreider, Paul D. Miller, and Warren T. Ford. "Poly(propylene imine) dendrimer complexes of Cu(II), Zn(II), and Co(III) as catalysts of hydrolysis of bis-(p-nitrophenyl) phosphate." Reactive and Functional Polymers 41, no. 1-3 (1999): 205–12. http://dx.doi.org/10.1016/s1381-5148(99)00025-5.

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17

Cavallo, Luigi, and Franca Fraternali. "A Molecular Dynamics Study of the First Five Generations of Poly(Propylene Imine) Dendrimers Modified with N-tBoc-L-Phenylalanine." Chemistry - A European Journal 4, no. 5 (1998): 927–34. http://dx.doi.org/10.1002/(sici)1521-3765(19980515)4:5<927::aid-chem927>3.0.co;2-w.

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18

Teo, Lay-Lian, Sau-Leng Sin, and Chee-Yan Chan. "ESCA and TOF-SIMS Study on Oxidised and Reduced Polypyrrole-Poly(Vinylsulfonic Acid, Sodium Salt) Films Synthesized on Ti Electrodes." Journal of Nanomaterials 2010 (2010): 1–10. http://dx.doi.org/10.1155/2010/385617.

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We had previously reported on a surface analysis investigation of electrochemically synthesized, both oxidized and reduced, polypyrrole-poly-4-styrenesulfonate free-standing films (Sin et al., 2000). We apply the same techniques that we used earlier (Sin et al., 2000) to study polypyrrole-poly(vinylsulfonic acid, sodium salt) (PPy-PVS) free-standing films. Electron Spectroscopy for Chemical Analysis (ESCA) and Time of Flight Secondary Ion Mass Spectrometry (TOF-SIMS) were used in the surface morphology study of oxidized and reduced PPy-PVS composite films. ESCA spectra seem to indicate that th

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19

Ramani, R., V. Das, A. Singh, R. Ramachandran, G. Amarendra, and S. Alam. "Free Volume Study on the Origin of Dielectric Constant in a Fluorine-Containing Polyimide Blend: Poly(vinylidene fluoride-co-hexafluoro propylene)/Poly(ether imide)." Journal of Physical Chemistry B 118, no. 42 (2014): 12282–96. http://dx.doi.org/10.1021/jp506039y.

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