메뉴 건너뛰기




Volumn 53, Issue 49, 2014, Pages 18761-18774

Degradation of chemical threats by brominated polymer networks

Author keywords

[No Author keywords available]

Indexed keywords

CROSSLINKING; CYCLIC VOLTAMMETRY; DIMETHYLFORMAMIDE; ETHANE; ETHYLENE; FREE RADICALS; HYDRAZINE; OXIDATION; POLYMERS; REDOX REACTIONS; SULFUR COMPOUNDS; SWELLING; UREA;

EID: 84916613865     PISSN: 08885885     EISSN: 15205045     Source Type: Journal    
DOI: 10.1021/ie501055g     Document Type: Article
Times cited : (31)

References (88)
  • 1
    • 0024030381 scopus 로고
    • Poly(N -bromoacrylamide): A new polymeric recyclable oxidizing and brominating reagent
    • George, B. K.; Pillai, V. N. R. Poly(N -bromoacrylamide): A new polymeric recyclable oxidizing and brominating reagent Macromolecules 1988, 21, 1867-1870
    • (1988) Macromolecules , vol.21 , pp. 1867-1870
    • George, B.K.1    Pillai, V.N.R.2
  • 2
    • 0036173305 scopus 로고    scopus 로고
    • The degradation of organophosphorus pesticides in natural waters: A critical review
    • Pehkonen, S. O.; Zhang, Q. The degradation of organophosphorus pesticides in natural waters: A critical review Crit. Rev. Environ. Sci. Technol. 2002, 32, 17-72
    • (2002) Crit. Rev. Environ. Sci. Technol. , vol.32 , pp. 17-72
    • Pehkonen, S.O.1    Zhang, Q.2
  • 3
    • 0034120856 scopus 로고    scopus 로고
    • A review of the natural occurrence, synthetic production and use of carcinogenic hydrazines and related chemicals
    • Toth, B. A review of the natural occurrence, synthetic production and use of carcinogenic hydrazines and related chemicals In Vivo. 2000, 14, 299-319
    • (2000) In Vivo. , vol.14 , pp. 299-319
    • Toth, B.1
  • 4
    • 0022882605 scopus 로고
    • Polymer-bound oxidizing agents
    • Taylor, R. T. Polymer-bound oxidizing agents ACS Symp. Ser. 1986, 308, 132-154
    • (1986) ACS Symp. Ser. , vol.308 , pp. 132-154
    • Taylor, R.T.1
  • 6
    • 61649103349 scopus 로고    scopus 로고
    • New refreshable N -halamine polymeric biocides: N-chlorination of acyclic amide grafted cellulose
    • Liu, S.; Sun, G. New refreshable N -halamine polymeric biocides: N-chlorination of acyclic amide grafted cellulose Ind. Eng. Chem. Res. 2009, 48, 613-618
    • (2009) Ind. Eng. Chem. Res. , vol.48 , pp. 613-618
    • Liu, S.1    Sun, G.2
  • 7
    • 84874820639 scopus 로고    scopus 로고
    • Antimicrobial N -halamine polymers and coatings: A review of their synthesis, characterization, and applications
    • Hui, F.; Debiemme-Chouvy, C. Antimicrobial N -halamine polymers and coatings: A review of their synthesis, characterization, and applications Biomacromolecules 2013, 14, 585-560
    • (2013) Biomacromolecules , vol.14 , pp. 585-560
    • Hui, F.1    Debiemme-Chouvy, C.2
  • 8
    • 84857999313 scopus 로고    scopus 로고
    • Residual disinfection with N -halamine based antimicrobial paints
    • Kocer, H. B. Residual disinfection with N -halamine based antimicrobial paints Prog. Org. Coat. 2012, 74, 100-105
    • (2012) Prog. Org. Coat. , vol.74 , pp. 100-105
    • Kocer, H.B.1
  • 9
    • 66649094787 scopus 로고    scopus 로고
    • A study on melt grafting of N -halamine moieties onto polyethylene and their antibacterial activities
    • Badrossamay, M. R.; Sun, G. A study on melt grafting of N -halamine moieties onto polyethylene and their antibacterial activities Macromolecules 2009, 42, 1948-1954
    • (2009) Macromolecules , vol.42 , pp. 1948-1954
    • Badrossamay, M.R.1    Sun, G.2
  • 10
    • 73849093320 scopus 로고    scopus 로고
    • Synthesis and applications of cross-linked poly(N -bromomaleimide) in oxidation of various organic compounds
    • Tamami, B.; Shirazi, A. N.; Ebrahimzadeh, F. Synthesis and applications of cross-linked poly(N -bromomaleimide) in oxidation of various organic compounds Iran. Polym. J. 2009, 18, 957-967
    • (2009) Iran. Polym. J. , vol.18 , pp. 957-967
    • Tamami, B.1    Shirazi, A.N.2    Ebrahimzadeh, F.3
  • 12
    • 78249247092 scopus 로고    scopus 로고
    • Antimicrobial coatings based on hydantoin-containing polymer networks for textiles
    • Volkmann, A.; Ghosh, S. Antimicrobial coatings based on hydantoin-containing polymer networks for textiles J. Appl. Polym. Sci. 2011, 119, 1646-1651
    • (2011) J. Appl. Polym. Sci. , vol.119 , pp. 1646-1651
    • Volkmann, A.1    Ghosh, S.2
  • 15
    • 24744434727 scopus 로고    scopus 로고
    • Poly(vinylpyrrolidone)-bromine complex: A mild and efficient reagent for selective bromination of alkenes and oxidation of alcohols
    • Lakouraj, M. M.; Tajbakhsh, M.; Mokhtary, M. Poly(vinylpyrrolidone)-bromine complex: A mild and efficient reagent for selective bromination of alkenes and oxidation of alcohols J. Chem. Res. 2005, 8, 481-483
    • (2005) J. Chem. Res. , vol.8 , pp. 481-483
    • Lakouraj, M.M.1    Tajbakhsh, M.2    Mokhtary, M.3
  • 16
    • 23844487369 scopus 로고    scopus 로고
    • Bromine complexes of polyvinylpyrrolidone supports: A mild reagent for the transformation of α-oxoketene dithioacetals to β-oxothiolesters
    • Mathew, P.; Nair, S. K.; Sreedhar, K. M.; Pillai, V. N. R.; Asokan, C. V. Bromine complexes of polyvinylpyrrolidone supports: A mild reagent for the transformation of α-oxoketene dithioacetals to β-oxothiolesters Synth. Commun. 2005, 35, 2157-2161
    • (2005) Synth. Commun. , vol.35 , pp. 2157-2161
    • Mathew, P.1    Nair, S.K.2    Sreedhar, K.M.3    Pillai, V.N.R.4    Asokan, C.V.5
  • 17
    • 33746320124 scopus 로고    scopus 로고
    • Poly(N -vinylpyrrolidone)-hydrotribromide: A new gel-type resin for alcohol oxidation and alkene dibromination
    • Koshy, E. P.; Zacharias, J.; Pillai, V. N. R. Poly(N -vinylpyrrolidone)-hydrotribromide: A new gel-type resin for alcohol oxidation and alkene dibromination React. Funct. Polym. 2006, 66, 845-850
    • (2006) React. Funct. Polym. , vol.66 , pp. 845-850
    • Koshy, E.P.1    Zacharias, J.2    Pillai, V.N.R.3
  • 18
    • 33947100841 scopus 로고    scopus 로고
    • Polyvinylpolypyrrolidone-bromine complex, mild and efficient polymeric reagent for selective deprotection and oxidative deprotection of silylethers
    • Lakouraj, M. M.; Mokhtary, M. Polyvinylpolypyrrolidone-bromine complex, mild and efficient polymeric reagent for selective deprotection and oxidative deprotection of silylethers Lett. Org. Chem. 2007, 4, 64-67
    • (2007) Lett. Org. Chem. , vol.4 , pp. 64-67
    • Lakouraj, M.M.1    Mokhtary, M.2
  • 19
    • 0021587854 scopus 로고
    • Polymers of N -vinylpyrrolidone: Synthesis, characterization and uses
    • Haaf, F.; Sanner, A.; Straub, F. Polymers of N -vinylpyrrolidone: Synthesis, characterization and uses Polym. J. 1985, 17, 143-152
    • (1985) Polym. J. , vol.17 , pp. 143-152
    • Haaf, F.1    Sanner, A.2    Straub, F.3
  • 20
    • 0018580927 scopus 로고
    • Structure of polyvinylpyrrolidone-iodine (povidone-iodine)
    • Schenck, H.-U.; Simak, P.; Haedicke, E. Structure of polyvinylpyrrolidone-iodine (povidone-iodine) J. Pharm. Sci. 1979, 68, 1505-1509
    • (1979) J. Pharm. Sci. , vol.68 , pp. 1505-1509
    • Schenck, H.-U.1    Simak, P.2    Haedicke, E.3
  • 21
    • 78249247092 scopus 로고    scopus 로고
    • Antimicrobial coatings based on hydantoin-containing polymer networks for textiles
    • Volkmann, A.; Ghosh, S. Antimicrobial coatings based on hydantoin-containing polymer networks for textiles J. Appl. Polym. Sci. 2011, 119, 1646-1651
    • (2011) J. Appl. Polym. Sci. , vol.119 , pp. 1646-1651
    • Volkmann, A.1    Ghosh, S.2
  • 23
    • 33747857518 scopus 로고
    • Brominations with N -bromosuccinimide and related compounds. The Wohl-Ziegler reaction
    • Djerassi, C. Brominations with N -bromosuccinimide and related compounds. The Wohl-Ziegler reaction Chem. Rev. 1948, 43, 271-317
    • (1948) Chem. Rev. , vol.43 , pp. 271-317
    • Djerassi, C.1
  • 24
    • 0001698723 scopus 로고
    • N -Bromosuccinimide. I. Allylic bromination, a general survey of reaction variables
    • Dauben, H. J.; Layton, L.; McCoy, L. L. N -Bromosuccinimide. I. Allylic bromination, a general survey of reaction variables J. Am. Chem. Soc. 1959, 81, 4863-4873
    • (1959) J. Am. Chem. Soc. , vol.81 , pp. 4863-4873
    • Dauben, H.J.1    Layton, L.2    McCoy, L.L.3
  • 25
    • 33947457416 scopus 로고
    • Reactions of N -bromosuccinimide. II
    • Barnes, R. A.; Buckwalter, G. R. Reactions of N -bromosuccinimide. II J. Am. Chem. Soc. 1951, 73, 3858-3861
    • (1951) J. Am. Chem. Soc. , vol.73 , pp. 3858-3861
    • Barnes, R.A.1    Buckwalter, G.R.2
  • 26
    • 0001494364 scopus 로고
    • Reaction of N -bromosuccinimide with secondary alcohols
    • Stuckwisch, C. G.; Hammer, G. G.; Blau, N. F. Reaction of N -bromosuccinimide with secondary alcohols J. Org. Chem. 1957, 22, 1678-1680
    • (1957) J. Org. Chem. , vol.22 , pp. 1678-1680
    • Stuckwisch, C.G.1    Hammer, G.G.2    Blau, N.F.3
  • 27
    • 0012005418 scopus 로고
    • N -Bromosuccinimide oxidation of silyl ethers
    • Pinnick, H. W.; Lajis, N. H. N -Bromosuccinimide oxidation of silyl ethers J. Org. Chem. 1978, 43, 371-372
    • (1978) J. Org. Chem. , vol.43 , pp. 371-372
    • Pinnick, H.W.1    Lajis, N.H.2
  • 28
    • 33751156727 scopus 로고
    • Selective oxidation of alcohols using the 1:1 complex of N -bromosuccinimide and tetrabutylammonium iodide
    • Beebe, T. R.; Boyd, L.; Fonkeng, S. B.; Horn, J.; Mooney, T. M.; Saderholm, M. J.; Skidmore, M. V. Selective oxidation of alcohols using the 1:1 complex of N -bromosuccinimide and tetrabutylammonium iodide J. Org. Chem. 1995, 60, 6602-6603
    • (1995) J. Org. Chem. , vol.60 , pp. 6602-6603
    • Beebe, T.R.1    Boyd, L.2    Fonkeng, S.B.3    Horn, J.4    Mooney, T.M.5    Saderholm, M.J.6    Skidmore, M.V.7
  • 29
    • 0001235190 scopus 로고
    • N -Bromosuccinimide in acetonitrile: A mild and regiospecific nuclear brominating reagent for methoxybenzenes and naphthalenes
    • Carreno, M. C.; Ruano, J. L. G.; Sanz, G.; Toledo, M. A.; Urbano, A. N -Bromosuccinimide in acetonitrile: A mild and regiospecific nuclear brominating reagent for methoxybenzenes and naphthalenes J. Org. Chem. 1995, 60, 5328-5331
    • (1995) J. Org. Chem. , vol.60 , pp. 5328-5331
    • Carreno, M.C.1    Ruano, J.L.G.2    Sanz, G.3    Toledo, M.A.4    Urbano, A.5
  • 30
    • 0010725658 scopus 로고
    • Oxidative degradation of imidazoles by bromine or N -bromosuccinimide
    • Schmir, G. L.; Cohen, L. A. Oxidative degradation of imidazoles by bromine or N -bromosuccinimide Biochemistry 1965, 4, 533-538
    • (1965) Biochemistry , vol.4 , pp. 533-538
    • Schmir, G.L.1    Cohen, L.A.2
  • 31
    • 84916595408 scopus 로고    scopus 로고
    • Lewis base catalysis by thiourea: N -bromosuccinimide-mediated oxidation of alcohols
    • Tripathi, C. B.; Mukherjee, S. Lewis base catalysis by thiourea: N -bromosuccinimide-mediated oxidation of alcohols J. Org. Chem. 2011, 50, 12421-1242
    • (2011) J. Org. Chem. , vol.50 , pp. 12421-21242
    • Tripathi, C.B.1    Mukherjee, S.2
  • 32
    • 80855144431 scopus 로고    scopus 로고
    • Kinetics and mechanism of oxidation of l-proline by N -bromosuccinimide in aqueous acidic medium
    • Abdel-Hady, A. E. M. Kinetics and mechanism of oxidation of l-proline by N -bromosuccinimide in aqueous acidic medium Ind. Eng. Chem. Res. 2011, 50, 12421-12425
    • (2011) Ind. Eng. Chem. Res. , vol.50 , pp. 12421-12425
    • Abdel-Hady, A.E.M.1
  • 33
    • 0016559512 scopus 로고
    • Maleimide polymers. 111. Color reactions and kinetics
    • Haas, H. C.; Moreau, R. D. Maleimide polymers. 111. Color reactions and kinetics J.Poly.Sci.A 1975, 13, 2327-2334
    • (1975) J.Poly.Sci.A , vol.13 , pp. 2327-2334
    • Haas, H.C.1    Moreau, R.D.2
  • 35
    • 0025510729 scopus 로고
    • Synthesis and characterization of poly(N -tert-alkylmaleimide)s
    • Otsu, T.; Matsumoto, A.; Tatsumi, A. Synthesis and characterization of poly(N -tert-alkylmaleimide)s Polym. Bull. 1990, 24, 467-474
    • (1990) Polym. Bull. , vol.24 , pp. 467-474
    • Otsu, T.1    Matsumoto, A.2    Tatsumi, A.3
  • 36
    • 0027044048 scopus 로고
    • Polymaleimides bearing a readily hydrolyzable side group: Synthesis and polymerization of N -trialkylsilylmaleimides and characterization of the polymers
    • Matsumoto, A.; Oki, Y.; Otsu, T. Polymaleimides bearing a readily hydrolyzable side group: Synthesis and polymerization of N -trialkylsilylmaleimides and characterization of the polymers Polym. J. 1992, 24, 679-688
    • (1992) Polym. J. , vol.24 , pp. 679-688
    • Matsumoto, A.1    Oki, Y.2    Otsu, T.3
  • 37
    • 79953086400 scopus 로고    scopus 로고
    • A simple and practical solvent-free preparation of polymaleimide
    • Zhang, X. R.; Tang, B. T.; Zhang, S. F. A simple and practical solvent-free preparation of polymaleimide Molecules. 2011, 16, 1981-1986
    • (2011) Molecules. , vol.16 , pp. 1981-1986
    • Zhang, X.R.1    Tang, B.T.2    Zhang, S.F.3
  • 38
    • 0000855559 scopus 로고    scopus 로고
    • Solventless attachment of long-chain molecules to poly(ethylene- alt -maleic anhydride) copolymer surfaces
    • Evenson, S. A.; Badyal, J. P. S. Solventless attachment of long-chain molecules to poly(ethylene- alt -maleic anhydride) copolymer surfaces J. Phys. Chem. B 1998, 102, 5500-5502
    • (1998) J. Phys. Chem. B , vol.102 , pp. 5500-5502
    • Evenson, S.A.1    Badyal, J.P.S.2
  • 39
    • 0034323238 scopus 로고    scopus 로고
    • Surface esterification of poly(ethylene- alt -maleic anhydride) copolymer
    • Evenson, S. A.; Fail, C. A.; Badyal, J. P. S. Surface esterification of poly(ethylene- alt -maleic anhydride) copolymer J. Phys. Chem. B 2000, 104, 10608-10611
    • (2000) J. Phys. Chem. B , vol.104 , pp. 10608-10611
    • Evenson, S.A.1    Fail, C.A.2    Badyal, J.P.S.3
  • 42
    • 34247174888 scopus 로고    scopus 로고
    • Copper (II) bromide: A simple and selective monobromination reagent for electron-rish aromatic compounds
    • Bhatt, S.; Nayak, S. K. Copper (II) bromide: a simple and selective monobromination reagent for electron-rish aromatic compounds Synth. Commun. 2007, 37, 1381-1388
    • (2007) Synth. Commun. , vol.37 , pp. 1381-1388
    • Bhatt, S.1    Nayak, S.K.2
  • 43
    • 37049052224 scopus 로고
    • The micro-determination of hydrazine salts and certain derivatives
    • Barakat, M. Z.; Shaker, M. The micro-determination of hydrazine salts and certain derivatives Analyst 1963, 88, 59-63
    • (1963) Analyst , vol.88 , pp. 59-63
    • Barakat, M.Z.1    Shaker, M.2
  • 44
    • 33947476517 scopus 로고
    • Determination of mixtures of hydrazine and 1,l-dimethyhydrazine
    • Malone, H. E. Determination of mixtures of hydrazine and 1,l-dimethyhydrazine Anal. Chem. 1961, 33, 575-577
    • (1961) Anal. Chem. , vol.33 , pp. 575-577
    • Malone, H.E.1
  • 45
    • 39749143889 scopus 로고    scopus 로고
    • Spectrophotometric determination of hydrazine using bromine and methyl red
    • George, M.; Nagaraja, K. S.; Balasubramanian, N. Spectrophotometric determination of hydrazine using bromine and methyl red Indian J. Chem. 2007, 46A, 1621-1624
    • (2007) Indian J. Chem. , vol.46 , pp. 1621-1624
    • George, M.1    Nagaraja, K.S.2    Balasubramanian, N.3
  • 46
    • 0027377453 scopus 로고
    • Synthesis, Absolute configuration, and analysis of malathion, malaoxon, and isomalathion enantiomers
    • Berkmant, C. E.; Thompson, C. M. Synthesis, Absolute configuration, and analysis of malathion, malaoxon, and isomalathion enantiomers Chem. Res. Toxicol. 1993, 6, 718-723
    • (1993) Chem. Res. Toxicol. , vol.6 , pp. 718-723
    • Berkmant, C.E.1    Thompson, C.M.2
  • 47
    • 80051626517 scopus 로고    scopus 로고
    • Montmorillonite functionalized with pralidoxime as a material for chemical protection against organophosphorous compounds
    • Bromberg, L.; Straut, C. M.; Centrone, A.; Wilusz, E.; Hatton, T. A. Montmorillonite functionalized with pralidoxime as a material for chemical protection against organophosphorous compounds ACS Appl. Mater. Interfaces 2011, 3, 1479-1484
    • (2011) ACS Appl. Mater. Interfaces , vol.3 , pp. 1479-1484
    • Bromberg, L.1    Straut, C.M.2    Centrone, A.3    Wilusz, E.4    Hatton, T.A.5
  • 48
    • 0018454395 scopus 로고
    • Crosslinking aqueous poly(vinyl pyrrolidone) solutions by persulfate
    • Anderson, C. C.; Rodrigues, F.; Thurston, D. A. Crosslinking aqueous poly(vinyl pyrrolidone) solutions by persulfate J. Appl. Polym. Sci. 1979, 23, 2453-2462
    • (1979) J. Appl. Polym. Sci. , vol.23 , pp. 2453-2462
    • Anderson, C.C.1    Rodrigues, F.2    Thurston, D.A.3
  • 49
    • 0004669023 scopus 로고
    • Electrochemical reduction of N -bromosuccinimide. Reaction mechanism for formation of the succinimidyl radical
    • Barry, J. E.; Finkelstein, M.; Moore, W. M.; Ross, S. D.; Eberson, L.; Jonsson, L. Electrochemical reduction of N -bromosuccinimide. Reaction mechanism for formation of the succinimidyl radical J. Org. Chem. 1982, 47, 1292-1298
    • (1982) J. Org. Chem. , vol.47 , pp. 1292-1298
    • Barry, J.E.1    Finkelstein, M.2    Moore, W.M.3    Ross, S.D.4    Eberson, L.5    Jonsson, L.6
  • 50
    • 84857418827 scopus 로고    scopus 로고
    • Voltammetry on N -bromosuccinimide in hexafluoropropan-2-ol
    • Haque, I. U.; Akram, W.; Tariq, M.; Khan, A. Voltammetry on N -bromosuccinimide in hexafluoropropan-2-ol Electrochem. Sci. Trans. 2011, 33, 41-48
    • (2011) Electrochem. Sci. Trans. , vol.33 , pp. 41-48
    • Haque, I.U.1    Akram, W.2    Tariq, M.3    Khan, A.4
  • 51
    • 0034454662 scopus 로고    scopus 로고
    • A comparative evaluation of operating conditions for the electrochemical bromination and chlorination of succinimide
    • Krishnamoorthy, S.; Srinivasan, R. K.; Noel, M. A comparative evaluation of operating conditions for the electrochemical bromination and chlorination of succinimide Bull. Electrochem. 2000, 16, 544-550
    • (2000) Bull. Electrochem. , vol.16 , pp. 544-550
    • Krishnamoorthy, S.1    Srinivasan, R.K.2    Noel, M.3
  • 52
    • 0013347407 scopus 로고
    • The electrochemical reduction of succinimide
    • Moore, W. M.; Finkelstein, M.; Ross, S. D. The electrochemical reduction of succinimide Tetrahedron 1980, 36, 727-730
    • (1980) Tetrahedron , vol.36 , pp. 727-730
    • Moore, W.M.1    Finkelstein, M.2    Ross, S.D.3
  • 53
    • 84864358107 scopus 로고    scopus 로고
    • Electrochemical detection of dopamine in the presence of ascorbic acid using PVP/graphene modified electrodes
    • Liu, Q.; Zhu, X.; Huo, Z.; He, X.; Liang, Y.; Xu, M. Electrochemical detection of dopamine in the presence of ascorbic acid using PVP/graphene modified electrodes Talanta 2012, 97, 557-562
    • (2012) Talanta , vol.97 , pp. 557-562
    • Liu, Q.1    Zhu, X.2    Huo, Z.3    He, X.4    Liang, Y.5    Xu, M.6
  • 54
    • 84870686754 scopus 로고    scopus 로고
    • Polyvinylpyrrolidone-enhanced electrochemical oxidation and detection of acyclovir
    • Wang, P.; Gan, T.; Zhang, J.; Luo, J.; Zhang, S. Polyvinylpyrrolidone-enhanced electrochemical oxidation and detection of acyclovir J. Mol. Liq. 2013, 177, 129-132
    • (2013) J. Mol. Liq. , vol.177 , pp. 129-132
    • Wang, P.1    Gan, T.2    Zhang, J.3    Luo, J.4    Zhang, S.5
  • 57
    • 0023732131 scopus 로고
    • Toxicity assessment of hydrazine fuels
    • Keller, W. C. Toxicity assessment of hydrazine fuels Aviat. Space Environ. Med. 1988, 59 (11 Pt 2) A100-106
    • (1988) Aviat. Space Environ. Med. , vol.59 , Issue.11 PART 2 , pp. 100-106
    • Keller, W.C.1
  • 58
    • 0346123006 scopus 로고    scopus 로고
    • Occupational exposure to hydrazines: Treatment of acute central nervous system toxicity
    • Zelnick, S. D.; Mattie, D. R.; Stepaniak, P. C. Occupational exposure to hydrazines: treatment of acute central nervous system toxicity Aviat. Space Environ. Med. 2003, 74, 1285-1291
    • (2003) Aviat. Space Environ. Med. , vol.74 , pp. 1285-1291
    • Zelnick, S.D.1    Mattie, D.R.2    Stepaniak, P.C.3
  • 59
    • 79151469086 scopus 로고    scopus 로고
    • Chemical reactions of polymer crosslinking and post-crosslinking at room and medium temperature
    • Tillet, G.; Boutevin, B.; Ameduri, B. Chemical reactions of polymer crosslinking and post-crosslinking at room and medium temperature Prog. Polym. Sci. 2011, 36, 191-217
    • (2011) Prog. Polym. Sci. , vol.36 , pp. 191-217
    • Tillet, G.1    Boutevin, B.2    Ameduri, B.3
  • 60
    • 2142777452 scopus 로고
    • Maleic hydrazide. I. Reactions with selected electrophilic reagents
    • Feuer, H.; Rubinstein, H. Maleic hydrazide. I. Reactions with selected electrophilic reagents J. Am. Chem. Soc. 1958, 80, 5873-5877
    • (1958) J. Am. Chem. Soc. , vol.80 , pp. 5873-5877
    • Feuer, H.1    Rubinstein, H.2
  • 61
    • 0013024395 scopus 로고
    • The reactions of maleic anhydride with hydrazine hydrate
    • Feuer, H.; White, E. H.; Wyman, J. E. The reactions of maleic anhydride with hydrazine hydrate J. Am. Chem. Soc. 1958, 80, 3790-3792
    • (1958) J. Am. Chem. Soc. , vol.80 , pp. 3790-3792
    • Feuer, H.1    White, E.H.2    Wyman, J.E.3
  • 62
    • 0024463538 scopus 로고    scopus 로고
    • Decompostion of hydrazine in aqueous solutions
    • Moliner, A. M.; Street, J. J. Decompostion of hydrazine in aqueous solutions J. Environ. Qual. 1998, 18, 483-487
    • (1998) J. Environ. Qual. , vol.18 , pp. 483-487
    • Moliner, A.M.1    Street, J.J.2
  • 63
    • 77953615567 scopus 로고    scopus 로고
    • Decontamination of VX surrogate malathion by atmospheric pressure radio-frequency plasma jet
    • Zhu, W.-C.; Wang, B.-R.; Xi, H.-L.; Pu, Y.-K. Decontamination of VX surrogate malathion by atmospheric pressure radio-frequency plasma jet Plasma Chem. Plasma Process. 2010, 30, 381-389
    • (2010) Plasma Chem. Plasma Process. , vol.30 , pp. 381-389
    • Zhu, W.-C.1    Wang, B.-R.2    Xi, H.-L.3    Pu, Y.-K.4
  • 64
    • 84886779651 scopus 로고    scopus 로고
    • Decontamination of chemical-warfare agent simulants by polymer surfaces doped with the singlet oxygen generator zinc octaphenoxyphthalocyanine
    • Gephart, R. T.; Coneski, P. N.; Wynne, J. H. Decontamination of chemical-warfare agent simulants by polymer surfaces doped with the singlet oxygen generator zinc octaphenoxyphthalocyanine ACS Appl. Mater. Interfaces 2013, 5, 10191-10200
    • (2013) ACS Appl. Mater. Interfaces , vol.5 , pp. 10191-10200
    • Gephart, R.T.1    Coneski, P.N.2    Wynne, J.H.3
  • 67
    • 0037112557 scopus 로고    scopus 로고
    • Hydrolysis of VX on concrete: Rate of degradation by direct surface interrogation using an ion trap secondary ion mass spectrometer
    • Groenewold, G. S.; Williams, J. M.; Appelhans, A. D.; Gresham, G. L.; Olson, J. E.; Jeffery, M. T.; Rowland, B. Hydrolysis of VX on concrete: Rate of degradation by direct surface interrogation using an ion trap secondary ion mass spectrometer Environ. Sci. Technol. 2002, 36, 4790-4794
    • (2002) Environ. Sci. Technol. , vol.36 , pp. 4790-4794
    • Groenewold, G.S.1    Williams, J.M.2    Appelhans, A.D.3    Gresham, G.L.4    Olson, J.E.5    Jeffery, M.T.6    Rowland, B.7
  • 68
    • 58149312985 scopus 로고    scopus 로고
    • Facile hydrolysis-based chemical destruction of the warfare agents VX, GB, and HD by alumina-supported fluoride reagents
    • Gershonov, E.; Columbus, I.; Zafrani, Y. Facile hydrolysis-based chemical destruction of the warfare agents VX, GB, and HD by alumina-supported fluoride reagents J. Org. Chem. 2009, 74, 329-338
    • (2009) J. Org. Chem. , vol.74 , pp. 329-338
    • Gershonov, E.1    Columbus, I.2    Zafrani, Y.3
  • 69
    • 80052814101 scopus 로고    scopus 로고
    • Destruction and detection of chemical warfare agents
    • Kim, K.; Tsay, O. G.; Atwood, D. A.; Churchill, D. G. Destruction and detection of chemical warfare agents Chem. Rev. 2011, 111, 5345-5403
    • (2011) Chem. Rev. , vol.111 , pp. 5345-5403
    • Kim, K.1    Tsay, O.G.2    Atwood, D.A.3    Churchill, D.G.4
  • 71
    • 0000020143 scopus 로고    scopus 로고
    • Oxidative hydrolysis of phosphorus (V) esters of thiols by peroxymonosulfate ion. Reactions of peroxymonosulfate ion with phosphorus (V) esters of thiols
    • Blaskó, A.; Bunton, C. A.; Kumar, A. Oxidative hydrolysis of phosphorus (V) esters of thiols by peroxymonosulfate ion. Reactions of peroxymonosulfate ion with phosphorus (V) esters of thiols J. Phys. Org. Chem. 1997, 10, 427-434
    • (1997) J. Phys. Org. Chem. , vol.10 , pp. 427-434
    • Blaskó, A.1    Bunton, C.A.2    Kumar, A.3
  • 74
    • 0032901947 scopus 로고    scopus 로고
    • Chemical detoxification of nerve agent VX
    • Yang, Y.-C. Chemical detoxification of nerve agent VX Acc. Chem. Res. 1999, 32, 109-115
    • (1999) Acc. Chem. Res. , vol.32 , pp. 109-115
    • Yang, Y.-C.1
  • 75
    • 33847185173 scopus 로고    scopus 로고
    • Decontamination of VX, GD, and HD on a surface using modified vaporized hydrogen peroxide
    • Wagner, G. W.; Sorrick, D. C.; Procell, L. R.; Brickhouse, M. D.; Mcvey, I. F.; Schwartz, L. I. Decontamination of VX, GD, and HD on a surface using modified vaporized hydrogen peroxide Langmuir 2007, 23, 1178-1186
    • (2007) Langmuir , vol.23 , pp. 1178-1186
    • Wagner, G.W.1    Sorrick, D.C.2    Procell, L.R.3    Brickhouse, M.D.4    McVey, I.F.5    Schwartz, L.I.6
  • 76
    • 21044451186 scopus 로고    scopus 로고
    • Detoxification of malathion a chemical warfare agent analog using oxygen activation at room temperature and pressure
    • Noradoun, C. E.; Mekmaysy, C. S.; Hutcheson, R. M.; Cheng, I. F. Detoxification of malathion a chemical warfare agent analog using oxygen activation at room temperature and pressure Green Chem. 2005, 7, 426-430
    • (2005) Green Chem. , vol.7 , pp. 426-430
    • Noradoun, C.E.1    Mekmaysy, C.S.2    Hutcheson, R.M.3    Cheng, I.F.4
  • 77
    • 33645959870 scopus 로고    scopus 로고
    • Oxidation as a pre-step in determination of organophosphorus compounds by the AChE-TLS bioassay
    • Kralj, M. B.; Trebše, P.; Franko, M. Oxidation as a pre-step in determination of organophosphorus compounds by the AChE-TLS bioassay Acta Chim. Slov. 2006, 53, 43-51
    • (2006) Acta Chim. Slov. , vol.53 , pp. 43-51
    • Kralj, M.B.1    Trebše, P.2    Franko, M.3
  • 79
    • 0027401406 scopus 로고
    • Monitoring of malathion and its impurities and environmental transformation products on surfaces and in air following an aerial application
    • Brown, M. A.; Petreas, M. X.; Okamoto, H. S.; Mischke, T. M.; Stephens, R. D. Monitoring of malathion and its impurities and environmental transformation products on surfaces and in air following an aerial application Environ. Sci. Technol. 1993, 27, 388-397
    • (1993) Environ. Sci. Technol. , vol.27 , pp. 388-397
    • Brown, M.A.1    Petreas, M.X.2    Okamoto, H.S.3    Mischke, T.M.4    Stephens, R.D.5
  • 80
    • 70249083735 scopus 로고    scopus 로고
    • Degradation behavior and products of malathion and chlorpyrifos spiked in apple juice by ultrasonic treatment
    • Zhang, Y.; Xiao, Z.; Chen, F.; Gea, Y.; Wu, J.; Hu, X. Degradation behavior and products of malathion and chlorpyrifos spiked in apple juice by ultrasonic treatment Ultrason. Sonochem. 2010, 17, 72-77
    • (2010) Ultrason. Sonochem. , vol.17 , pp. 72-77
    • Zhang, Y.1    Xiao, Z.2    Chen, F.3    Gea, Y.4    Wu, J.5    Hu, X.6
  • 81
    • 0000268381 scopus 로고
    • Role of water in polyoxometalate-catalyzed oxidations in nonaqueous media. Scope, kinetics, and mechanism of oxidation of thioether mustard (HD) analogs by tert -butyl hydroperoxide catalyzed by H5PV2Mo10O40
    • Gall, R. D.; Faraj, M.; Hill, C. L. Role of water in polyoxometalate-catalyzed oxidations in nonaqueous media. Scope, kinetics, and mechanism of oxidation of thioether mustard (HD) analogs by tert -butyl hydroperoxide catalyzed by H5PV2Mo10O40 Inorg. Chem. 1994, 33, 5015-5021
    • (1994) Inorg. Chem. , vol.33 , pp. 5015-5021
    • Gall, R.D.1    Faraj, M.2    Hill, C.L.3
  • 82
    • 0035923352 scopus 로고    scopus 로고
    • Catalytic aerobic oxidation of 2-chloroethyl ethylsulfide, a mustard simulant, under ambient conditions: Effect of solvents, ligands, and transition metals on reactivity
    • Boring, E.; Geletii, Y. V.; Hill, C. L. Catalytic aerobic oxidation of 2-chloroethyl ethylsulfide, a mustard simulant, under ambient conditions: Effect of solvents, ligands, and transition metals on reactivity J. Mol. Catal. A: Chem. 2001, 176, 49-63
    • (2001) J. Mol. Catal. A: Chem. , vol.176 , pp. 49-63
    • Boring, E.1    Geletii, Y.V.2    Hill, C.L.3
  • 83
    • 0037453361 scopus 로고    scopus 로고
    • 2/air-based oxidation of 2-chloroethyl ethyl sulfide at ambient temperature
    • 2/air-based oxidation of 2-chloroethyl ethyl sulfide at ambient temperature J. Mol. Catal. A: Chem. 2003, 197, 283-290
    • (2003) J. Mol. Catal. A: Chem. , vol.197 , pp. 283-290
    • Okun, N.M.1    Anderson, T.M.2    Hill, C.L.3
  • 84
    • 51049100365 scopus 로고    scopus 로고
    • Catalysts for aerobic decontamination of chemical warfare agents under ambient conditions
    • Hill, C. L.; Okun, N. M.; Hillesheim, D. A.; Geletii, Y. V. Catalysts for aerobic decontamination of chemical warfare agents under ambient conditions ACS Symp. Ser. 2007, 980, 198-209
    • (2007) ACS Symp. Ser. , vol.980 , pp. 198-209
    • Hill, C.L.1    Okun, N.M.2    Hillesheim, D.A.3    Geletii, Y.V.4
  • 86
    • 84871824084 scopus 로고    scopus 로고
    • Chemical warfare agent simulants in gamble's fluid: Is the fluid toxic? Can it be made safer by inclusion of solid nanocrystalline metal oxides?
    • Article ID 641620
    • Karote, D.; Walker, B.; Dai, H.; Krishnamoorthi, R.; Voo, J.; Rajagopalan, S. J. Chemical warfare agent simulants in gamble's fluid: Is the fluid toxic? Can it be made safer by inclusion of solid nanocrystalline metal oxides? J. Chem. 2013, Article ID 641620, 14 pages, http://dx.doi.org/10.1155/2013/641620.
    • (2013) J. Chem. , pp. 14
    • Karote, D.1    Walker, B.2    Dai, H.3    Krishnamoorthi, R.4    Voo, J.5    Rajagopalan, S.J.6
  • 87
    • 33751552816 scopus 로고
    • A comparison of the oxidative reactivities of mustard (2,2′-dichlorodiethyl sulfide) and bivalent sulfides
    • Yang, Y.-C.; Szafraniec, L. L.; Beaudry, W. T. A comparison of the oxidative reactivities of mustard (2,2′-dichlorodiethyl sulfide) and bivalent sulfides J. Org. Chem. 1990, 55, 3664-3666
    • (1990) J. Org. Chem. , vol.55 , pp. 3664-3666
    • Yang, Y.-C.1    Szafraniec, L.L.2    Beaudry, W.T.3
  • 88
    • 18444419379 scopus 로고
    • Kinetics and mechanism of the hydrolysis of 2-chloroethyl sulfides
    • Yang, Y.-C.; Szafraniec, L. L.; Beaudry, W. T.; Ward, J. R. Kinetics and mechanism of the hydrolysis of 2-chloroethyl sulfides J. Org. Chem. 1988, 53, 3293-3297
    • (1988) J. Org. Chem. , vol.53 , pp. 3293-3297
    • Yang, Y.-C.1    Szafraniec, L.L.2    Beaudry, W.T.3    Ward, J.R.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.