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Artigos de revistas sobre o tema "Triaziridine"

Autor: Grafiati
Publicado: 14 de dezembro de 2024

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1

Hilpert, Hans, Lienhard Hoesch e Andr� S. Dreiding. "Triaziridine. 6. Mitteilung. Substituententransformationen an Triaziridinen". Helvetica Chimica Acta 69, n.º 8 (10 de dezembro de 1986): 2087–97. http://dx.doi.org/10.1002/hlca.19860690833.

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2

Hilpert, Hans, e André S. Dreiding. "Triaziridine. 9. Mitteilung. Ringöffnungen von Triaziridinen". Helvetica Chimica Acta 71, n.º 1 (3 de fevereiro de 1988): 277–91. http://dx.doi.org/10.1002/hlca.19880710132.

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3

Hilpert, Hans, Lienhard Hoesch e Andr� S. Dreiding. "Triaziridine 8. Mitteilung. Zur Acylierung Von Dialkyl-triaziridinen". Helvetica Chimica Acta 70, n.º 2 (18 de março de 1987): 390–95. http://dx.doi.org/10.1002/hlca.19870700217.

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4

Kaupp, Gerd, Oswald Dengler, Klaus Burger e Silvia Rottegger. "Stabile Triaziridine". Angewandte Chemie 97, n.º 4 (abril de 1985): 329–30. http://dx.doi.org/10.1002/ange.19850970420.

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5

Hilpert, Hans, Lienhard Hoesch e Andr� S. Dreiding. "Triaziridine 7. Mitteilung. Stabile pyramidale Konfigurationen an den Stickstoff-Atomen von Dialkyl-und Trialkyl-triaziridinen". Helvetica Chimica Acta 70, n.º 2 (18 de março de 1987): 381–89. http://dx.doi.org/10.1002/hlca.19870700216.

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6

Kaupp, Gerd, Jens A. Döhle, Klaus Burger, Paul Rademacher e Rainer Poppek. "The lone-pair orbitals of triaziridine". Journal of Physical Organic Chemistry 1, n.º 5 (setembro de 1988): 267–73. http://dx.doi.org/10.1002/poc.610010504.

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7

Kaupp, Gerd, e Jens A. Döhle. "An Azimine-Triaziridine Transformation by Laser Photolysis". Angewandte Chemie International Edition in English 25, n.º 9 (setembro de 1986): 828–30. http://dx.doi.org/10.1002/anie.198608281.

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8

Chi, Weijie, Butong Li e Haishun Wu. "Density function theory study on energetic nitro-triaziridine derivatives". Structural Chemistry 24, n.º 2 (3 de julho de 2012): 375–81. http://dx.doi.org/10.1007/s11224-012-0083-2.

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9

Hilpert, Hans, Lienhard Hoesch e André S. Dreiding. "Triaziridine. 4. Mitteilung. Synthese voncis-2,3-Diisopropyltriaziridin-1-carbonsäureestern". Helvetica Chimica Acta 68, n.º 6 (25 de setembro de 1985): 1691–97. http://dx.doi.org/10.1002/hlca.19850680624.

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10

Karahodza, Anida, Karen J. Knaus e David W. Ball. "Cyclic triamines as potential high energy materials. Thermochemical properties of triaziridine and triazirine". Journal of Molecular Structure: THEOCHEM 732, n.º 1-3 (novembro de 2005): 47–53. http://dx.doi.org/10.1016/j.theochem.2005.07.004.

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11

Chen, Po-Cheng, Shih-Chieh Wang, Chia-Yu Huang, Jen-Taut Yeh e Kan-Nan Chen. "New crosslinked polymer from a rapid polymerization of acrylic acid with triaziridine-containing compound". Journal of Applied Polymer Science 104, n.º 2 (2007): 809–15. http://dx.doi.org/10.1002/app.25548.

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12

Peverati, Roberto, Jay S. Siegel e Kim K. Baldridge. "Ab initio quantum chemical computations of substituent effects on triaziridine strain energy and heat of formation". Physical Chemistry Chemical Physics 11, n.º 14 (2009): 2387. http://dx.doi.org/10.1039/b816782f.

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13

Engel, Paul S., Li Pan, Kenton H. Whitmire, Ilse Guzman-Jimenez, M. Robert Willcott e William B. Smith. "Mechanistic Studies of a Linear Trisazoalkane, a New Azimine, and a Bicyclic Triaziridine. Azoalkane Homolysis into Seven Fragments". Journal of Organic Chemistry 65, n.º 4 (fevereiro de 2000): 1016–21. http://dx.doi.org/10.1021/jo991439g.

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14

Song, Hua-Jie, He-Ming Xiao, Hai-Shan Dong e Wei-Hua Zhu. "Cooperative Effects and Strengths of Hydrogen Bonds in Open-Chaincis-Triaziridine Clusters (n= 2−8): A DFT Investigation". Journal of Physical Chemistry A 110, n.º 6 (fevereiro de 2006): 2225–30. http://dx.doi.org/10.1021/jp055385s.

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15

Engel, Paul S., Li Pan, Kenton H. Whitmire, Ilse Guzman-Jimenez, M. Robert Willcott e William B. Smith. "ChemInform Abstract: Mechanistic Studies of a Linear Trisazoalkane, a New Azimine, and a Bicyclic Triaziridine. Azoalkane Homolysis into Seven Fragments." ChemInform 31, n.º 21 (8 de junho de 2010): no. http://dx.doi.org/10.1002/chin.200021072.

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16

Alcamí, Manuel, Otilia Mó, Manuel Yáñez, Ibon Alkorta e José Elguero. "Triaziridine and tetrazetidine vs. cyclic water trimer and tetramer: A computational approach to the relationship between molecular and supramolecular conformational analysis". Physical Chemistry Chemical Physics 4, n.º 11 (30 de abril de 2002): 2123–29. http://dx.doi.org/10.1039/b108270c.

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17

Kaupp, Gerd, Oswald Dengler, Klaus Burger e Silvia Rottegger. "Stable Triaziridines". Angewandte Chemie International Edition in English 24, n.º 4 (abril de 1985): 341–42. http://dx.doi.org/10.1002/anie.198503411.

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18

Hilpert, Hans, e Roger Hollenstein. "15N-NMR Spectroscopic Characterization of Triaziridines". Helvetica Chimica Acta 69, n.º 1 (5 de fevereiro de 1986): 136–40. http://dx.doi.org/10.1002/hlca.19860690116.

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19

Kaupp, Gerd, e Jens A. Döhle. "Eine Azimin-Triaziridin-Umwandlung durch Laserphotolyse". Angewandte Chemie 98, n.º 9 (setembro de 1986): 814–15. http://dx.doi.org/10.1002/ange.19860980911.

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20

Gleiter, Rolf, Christoph Sigwart, Hermann Irngartinger, Stefan Gries, Wolfgang Marterer, Otmar Klingler e Horst Prinzbach. "cis,cis - Trialkyl-triaziridines photoelectron spectra - X-ray structural analysis". Tetrahedron Letters 29, n.º 2 (janeiro de 1988): 185–88. http://dx.doi.org/10.1016/s0040-4039(00)80048-9.

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21

Marterer, Wolfgang, Hans Fritz e Horst Prinzbach. "Stable cis,cis-trialkyl-triaziridines synthesis via azo/nitrene addition, n-oxidation". Tetrahedron Letters 28, n.º 45 (janeiro de 1987): 5497–500. http://dx.doi.org/10.1016/s0040-4039(00)96763-7.

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22

Burger, Klaus, Silvia Rottegger, Gerd Kaupp e Oswald Dengler. "Stabilization of small ring compounds by perfluoroalkyl groups synthesis of stable triaziridines". Journal of Fluorine Chemistry 29, n.º 1-2 (agosto de 1985): 133. http://dx.doi.org/10.1016/s0022-1139(00)83369-2.

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23

Kaneti, Jos�, Lienhard Hoesch e Andr� S. Dreiding. "Triaziridines. Part V. A semiempirical MNDO study of nitrogen inversion and amide rotation in Formyltriaziridines". Helvetica Chimica Acta 69, n.º 6 (10 de setembro de 1986): 1461–68. http://dx.doi.org/10.1002/hlca.19860690618.

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24

Hadjichristidis, Nikos, Jieai Fan, Changzheng Ju, Songjie Fan, Xia Li e Zhen Zhang. "Inverse Vulcanization of Aziridines: Enhancing Polysulfides for Superior Mechanical Strength and Adhesive Performance". Angewandte Chemie, 19 de novembro de 2024. http://dx.doi.org/10.1002/ange.202418764.

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This study introduces a novel approach to inverse vulcanization by utilizing a commercially available triaziridine crosslinker as an alternative to conventional olefin‐based crosslinkers. The model reactions reveal a self‐catalyzed ring‐opening of "unactivated" aziridine with elemental sulfur, forming oligosulfide‐functionalized diamines. The triaziridine‐derived polysulfides exhibit impressive mechanical properties, achieving a maximum stress of ~8.3 MPa and an elongation at break of ~107%. The incorporation of silicon dioxide (20 wt%) enhances the composite’s rigidity, yielding a Young's modulus of ~0.94 GPa. Furthermore, these polysulfides display excellent adhesion strength on various substrates, such as aluminum (~7.0 MPa), walnut (~9.6 MPa), and steel (~11.0 MPa), with substantial retention of adhesion strength (~3.3 MPa on steel) at −196 °C. The straightforward synthetic process, combined with the accessibility of the triaziridine crosslinker, emphasizes the potential for further innovations in sulfur polymer chemistry.
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25

Hadjichristidis, Nikos, Jieai Fan, Changzheng Ju, Songjie Fan, Xia Li e Zhen Zhang. "Inverse Vulcanization of Aziridines: Enhancing Polysulfides for Superior Mechanical Strength and Adhesive Performance". Angewandte Chemie International Edition, 19 de novembro de 2024. http://dx.doi.org/10.1002/anie.202418764.

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This study introduces a novel approach to inverse vulcanization by utilizing a commercially available triaziridine crosslinker as an alternative to conventional olefin‐based crosslinkers. The model reactions reveal a self‐catalyzed ring‐opening of "unactivated" aziridine with elemental sulfur, forming oligosulfide‐functionalized diamines. The triaziridine‐derived polysulfides exhibit impressive mechanical properties, achieving a maximum stress of ~8.3 MPa and an elongation at break of ~107%. The incorporation of silicon dioxide (20 wt%) enhances the composite’s rigidity, yielding a Young's modulus of ~0.94 GPa. Furthermore, these polysulfides display excellent adhesion strength on various substrates, such as aluminum (~7.0 MPa), walnut (~9.6 MPa), and steel (~11.0 MPa), with substantial retention of adhesion strength (~3.3 MPa on steel) at −196 °C. The straightforward synthetic process, combined with the accessibility of the triaziridine crosslinker, emphasizes the potential for further innovations in sulfur polymer chemistry.
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26

NGUYEN MINH-THO, NGUYEN MINH-THO, J. KANETI, L. HOESCH e A. S. DREIDING. "ChemInform Abstract: TRIAZIRIDINES. PART III. TRIAZIRIDINE, AZIMINE, AND TRIAZENE: A SCF STUDY OF OF THE ENERGY AND STRUCTURE OF N3H3 ISOMERS". Chemischer Informationsdienst 16, n.º 6 (12 de fevereiro de 1985). http://dx.doi.org/10.1002/chin.198506049.

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27

KAUPP, G., e J. A. DOEHLE. "ChemInform Abstract: An Azimine-Triaziridine Transformation by Laser Photolysis." ChemInform 18, n.º 3 (20 de janeiro de 1987). http://dx.doi.org/10.1002/chin.198703091.

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28

Naga, Naofumi, Tomoya Takenouchi e Tamaki Nakano. "Ring-Opening Polymerization of Triaziridine Compounds in Water: An Extremely Facile Method to Synthesize a Porous Polymer through Polymerization-Induced Phase Separation". ACS Macro Letters, 12 de abril de 2022, 603–7. http://dx.doi.org/10.1021/acsmacrolett.2c00110.

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29

HILPERT, H., L. HOESCH e A. S. DREIDING. "ChemInform Abstract: Triaziridines. Part 6. Substituent Transformations on Triaziridines." ChemInform 18, n.º 16 (21 de abril de 1987). http://dx.doi.org/10.1002/chin.198716188.

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30

HILPERT, H., L. HOESCH e A. S. DREIDING. "ChemInform Abstract: Triaziridines. Part 8. Acylation of Dialkyl-triaziridines." ChemInform 18, n.º 29 (21 de julho de 1987). http://dx.doi.org/10.1002/chin.198729152.

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31

HILPERT, H., e A. S. DREIDING. "ChemInform Abstract: Triaziridines. Part 9. Ring-Openings of Triaziridines." ChemInform 19, n.º 17 (26 de abril de 1988). http://dx.doi.org/10.1002/chin.198817084.

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32

KAUPP, G., O. DENGLER, K. BURGER e S. ROTTEGGER. "ChemInform Abstract: STABLE TRIAZIRIDINES". Chemischer Informationsdienst 16, n.º 31 (6 de agosto de 1985). http://dx.doi.org/10.1002/chin.198531210.

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33

HILPERT, H., L. HOESCH e A. S. DREIDING. "ChemInform Abstract: Triaziridines. Part 7. Stable Pyramidal Configurations at the Nitrogen Atoms of Dialkyl- and Trialkyl-triaziridines." ChemInform 18, n.º 28 (14 de julho de 1987). http://dx.doi.org/10.1002/chin.198728082.

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34

HILPERT, H., e R. HOLLENSTEIN. "ChemInform Abstract:15N NMR Spectroscopic Characterization of Triaziridines." Chemischer Informationsdienst 17, n.º 18 (6 de maio de 1986). http://dx.doi.org/10.1002/chin.198618053.

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35

HILPERT, H., L. HOESCH e A. S. DREIDING. "ChemInform Abstract: Triaziridines. Part 4. Synthesis of cis-2,3-Diisopropyltriaziridine-1-carboxylic Esters." Chemischer Informationsdienst 16, n.º 50 (17 de dezembro de 1985). http://dx.doi.org/10.1002/chin.198550161.

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36

KANETI, J., L. HOESCH e A. S. DREIDING. "ChemInform Abstract: Triaziridines. Part 5. A Semiempirical MNDO Study of Nitrogen Inversion and Amide Rotation in Formyltriaziridines." Chemischer Informationsdienst 17, n.º 52 (30 de dezembro de 1986). http://dx.doi.org/10.1002/chin.198652047.

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