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Journal articles on the topic 'Triphenyl phosphite'

Author: Grafiati

Published: 5 June 2025

Last updated: 1 August 2025

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1

Baran, J., N. A. Davydova, and M. Drozd. "Polymorphism of triphenyl phosphite." Journal of Chemical Physics 140, no. 10 (2014): 104512. http://dx.doi.org/10.1063/1.4867976.

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2

Jackson, WR, CG Lovel, P. Perlmutter, and AJ Smallridge. "The Stereochemistry of Organometallic Compounds. XXXI. Hydrocyanation of Alkynols." Australian Journal of Chemistry 41, no. 7 (1988): 1099. http://dx.doi.org/10.1071/ch9881099.

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The regioselectivity of hydrocyanation of a range of alkynols using nickel-based catalyst systems involving either triphenyl phosphite or α,α′-bis(diphenylphosphino)-o-xylene (phmep) has been investigated. The regioselectivity of the hydrocyanations involving the phosphine catalyst reflected dominant steric effects whereas results from the phosphite catalyst system showed some evidence for chelation control. Yields of nitriles from reactions based on the phosphite system were variable, whereas moderate to good yields of distilled products could be obtained consistently by using the phosphine -

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3

Wiedersich, J., A. Kudlik, J. Gottwald, G. Benini, I. Roggatz, and E. Rössler. "On Polyamorphism of Triphenyl Phosphite." Journal of Physical Chemistry B 101, no. 30 (1997): 5800–5803. http://dx.doi.org/10.1021/jp970848i.

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4

Sasseville, Denis, and Linda Moreau. "Allergic contact dermatitis from triphenyl phosphite." Contact Dermatitis 52, no. 3 (2005): 163–64. http://dx.doi.org/10.1111/j.0105-1873.2005.0548e.x.

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5

Alyea, E. C., G. Ferguson, and M. Zwikker. "cis-Tetracarbonylbis(triphenyl phosphite)molybdenum(0)." Acta Crystallographica Section C Crystal Structure Communications 50, no. 5 (1994): 676–78. http://dx.doi.org/10.1107/s0108270193013034.

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6

Alyea, E. C., G. Ferguson, and S. Q. Song. "fac-Tricarbonyltris(triphenyl phosphite)molybdenum(0)." Acta Crystallographica Section C Crystal Structure Communications 51, no. 11 (1995): 2238–42. http://dx.doi.org/10.1107/s0108270195006603.

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7

Krivchikov, Alexander, Ove Andersson, Oksana Korolyuk, and Oleksii Kryvchikov. "Thermal Conductivity of Solid Triphenyl Phosphite." Molecules 27, no. 23 (2022): 8399. http://dx.doi.org/10.3390/molecules27238399.

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The thermal conductivity, κ, of solid triphenyl phosphite was measured by using the transient hot-wire method, and its temperature and pressure dependencies were analyzed to understand heat transfer processes in the solid polymorphic phases, as well as in the glass and the exotic glacial state. Phase transformations and the structural order of the phases are discussed, and a transitional pressure–temperature diagram of triphenyl phosphite is presented. The thermal conductivity of both the crystalline and disordered states is described within the theory of two-channel heat transfer by phonons a

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8

Lee, Jin-Kyun, Rachel M. Williamson, Andrew B. Holmes, Edward J. Bush, and Ian F. McConvey. "A Study of the Heck Reaction in Non-Polar Hydrocarbon Solvents and in Supercritical Carbon Dioxide." Australian Journal of Chemistry 60, no. 8 (2007): 566. http://dx.doi.org/10.1071/ch07160.

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The effects of electronic and steric properties of phosphorus ligands on Heck reactions in supercritical CO2 and non-polar hydrocarbon solvents were studied. In Heck reactions between iodobenzene and butyl acrylate, higher yields were obtained with less electron-rich phosphine ligands. This trend was also observed with the electron-poor triphenyl phosphite. A range of sterically demanding phosphites were then investigated. Biphenyl-containing phosphites 8 and 13 were found to be highly effective. In the Heck reaction between the less-reactive bromobenzene and butyl acrylate, the bulky, electro

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9

Mendenhall, G. David, and Duane B. Priddy. "A Reexamination of the Ozone−Triphenyl Phosphite System. The Origin of Triphenyl Phosphate at Low Temperatures." Journal of Organic Chemistry 64, no. 16 (1999): 5783–86. http://dx.doi.org/10.1021/jo982339y.

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10

Mariani, Alberto, Sabina L. E. Mazzanti, and Saverio Russo. "Role of the reaction parameters in the direct synthesis of aromatic polyamides." Canadian Journal of Chemistry 73, no. 11 (1995): 1960–65. http://dx.doi.org/10.1139/v95-242.

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A thorough study, devoted to analyzing the role of various reaction parameters in the direct synthesis of poly(p-phenylene terephthalamide) and poly(p-benzamide), activated by triphenyl phosphite, is described. The effects of temperature, salt type and concentration, amount of triphenyl phosphite and its stepwise introduction, as well as monomer and reagent concentrations, are considered. The inherent viscosity values of the above aromatic polyamides are higher than those reported in the literature for analogous syntheses and are comparable to the values of typical samples obtained by the acyl

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11

Golovanov, Denis G., Konstantin A. Lyssenko, Mikhail Yu Antipin, Yakov S. Vygodskii, Elena I. Lozinskaya, and Alexander S. Shaplov. "Long-awaited polymorphic modification of triphenyl phosphite." CrystEngComm 7, no. 77 (2005): 465. http://dx.doi.org/10.1039/b505052a.

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12

Hédoux, A., Y. Guinet, and M. Descamps. "Raman signature of polyamorphism in triphenyl phosphite." Physical Review B 58, no. 1 (1998): 31–34. http://dx.doi.org/10.1103/physrevb.58.31.

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13

O'Driscoll, J. B., R. Marcus, and M. H. Beck. "Occupational allergic contact dermatitis from triphenyl phosphite." Contact Dermatitis 20, no. 5 (1989): 392–93. http://dx.doi.org/10.1111/j.1600-0536.1989.tb03190.x.

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14

Sasseville, D., and L. Moreau. "OCCUPATIONAL ALLERGIC CONTACT DERMATITIS FROM TRIPHENYL PHOSPHITE." Dermatitis 16, no. 2 (2005): 95. http://dx.doi.org/10.1097/01206501-200506000-00021.

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15

Senker, J., and E. Rössler. "Triphenyl phosphite: a candidate for liquid polyamorphism." Chemical Geology 174, no. 1-3 (2001): 143–56. http://dx.doi.org/10.1016/s0009-2541(00)00313-2.

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16

Shereshovets, V. V., N. M. Korotaeva, Yu I. Puzin, G. V. Leplyanin, and V. D. Komissarov. "Reaction of triphenyl phosphite ozonide with thioacetals." Reaction Kinetics & Catalysis Letters 42, no. 1 (1990): 39–46. http://dx.doi.org/10.1007/bf02137615.

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17

Shereshovets, V. V., N. M. Korotaeva, V. D. Komissarov, and G. A. Tolstikov. "Acid-catalyzed decomposition of triphenyl phosphite ozonide." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 34, no. 9 (1985): 1997. http://dx.doi.org/10.1007/bf00953958.

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18

Senker, Jürgen, and Jens Lüdecke. "Structure Determination for the Crystalline Phase of Triphenyl Phosphite by Means of Multi-Dimensional Solid-State NMR and X-Ray Diffraction." Zeitschrift für Naturforschung B 56, no. 11 (2001): 1089–99. http://dx.doi.org/10.1515/znb-2001-1101.

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The crystalline phase of triphenyl phosphite P(OC6H5)3 was investigated by means of 31P solid-state NMR and X-ray diffraction in a temperature range between 170 K and its melting point (Tm = 293 K). ID MAS NMR spectra exhibit one sharp central resonance indicating only one crystallographically unique molecule in the unit cell. A theoretical analysis concerning the shape of 2D exchange spectra for 1 = 1 /2 nuclei is presented. It is shown that if the exchange is caused by radio-frequency driven spin-diffusion, this technique allows to discriminate rotational symmetry elements in crystalline sol

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19

Suuronen, Katri, Maria Pesonen, Maj-Len Henriks-Eckerman, and Kristiina Aalto-Korte. "Triphenyl phosphite, a new allergen in polyvinylchloride gloves." Contact Dermatitis 68, no. 1 (2012): 42–49. http://dx.doi.org/10.1111/j.1600-0536.2012.02159.x.

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20

Levin, Edward D., Nadine C. Christopher, and Mohamed B. Abou‐Donia. "Triphenyl phosphite‐induced impairment of spatial alternation learning." Journal of Toxicology and Environmental Health 44, no. 4 (1995): 461–67. http://dx.doi.org/10.1080/15287399509531974.

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21

Torresani, C., E. Zendri, V. Vescovi, and G. De Panfilis. "Contact urticaria syndrome from occupational triphenyl phosphite exposure." Contact Dermatitis 48, no. 4 (2003): 237–38. http://dx.doi.org/10.1034/j.1600-0536.2003.00096.x.

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22

Young, C. S., S. W. Lee, and C. P. Cheng. "Photochemical reaction of dirhenium decacarbonyl with triphenyl phosphite." Journal of Organometallic Chemistry 282, no. 1 (1985): 85–93. http://dx.doi.org/10.1016/0022-328x(85)87144-8.

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23

Kazakov, D. V., N. N. Kabalnova, and V. V. Shereshovets. "Decomposition of triphenyl phosphite ozonide catalyzed by pyridine." Reaction Kinetics & Catalysis Letters 54, no. 2 (1995): 439–44. http://dx.doi.org/10.1007/bf02071038.

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24

Sinyashina, T. N., V. F. Mironov, E. N. Ofitserov, I. V. Konovalova, and A. N. Pudovik. "Reactions of triphenyl phosphite with di- and tribromoacetaldehydes." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 37, no. 7 (1988): 1483–85. http://dx.doi.org/10.1007/bf00962767.

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25

Nilsson, Kersti B., Mikhail Maliarik, and Ingmar Persson. "Coordination Chemistry of Solvated Metal Ions in Soft Donor Solvents." Molecules 30, no. 15 (2025): 3063. https://doi.org/10.3390/molecules30153063.

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The structures of hexaammine solvated indium(III) and thallium(III) ions in liquid ammonia solution are determined by EXAFS. Both complexes have regular octahedral coordination geometry with mean In-N and Tl-N bond distances of 2.23(1) and 2.29(2) Å, respectively. Ammine solvated thallium(III) in liquid ammonia is characterized with 205Tl NMR measurements. Solvents such as liquid ammonia, N,N-dimethylthioformamide (DMTF), trialkyl and triphenyl phosphite and phosphine are strong electron pair donors and thereby able to form bonds with a large covalent contribution with strong electron pair acc

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26

Tanabe, Ikue, Kiyoshi Takeda, and Katsuo Murata. "Thermal study on the impurity effect on thermodynamic stability of the glacial phase in triphenyl phosphite–triphenyl phosphate system." Thermochimica Acta 431, no. 1-2 (2005): 44–48. http://dx.doi.org/10.1016/j.tca.2005.01.033.

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27

Agrawal, Seema, and Anudeep Kumar Narula. "Facile synthesis of new thermally stable and organo-soluble polyamide-imides from phosphorus-containing aromatic amines and various dianhydrides." Journal of Polymer Engineering 33, no. 6 (2013): 509–20. http://dx.doi.org/10.1515/polyeng-2013-0100.

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Abstract Imide ring containing novel polyamide-imides (PAIs) were prepared by triphenyl phosphite-activated polycondensation of phosphorus-containing aromatic amines, bis(3-aminophenyl) isopropyl phosphine (BAP) and bis(3-aminophenyl) aminotolyl phosphine (TAP), with various diimide-diacids (DIDAS). All polymers were fully characterized by FTIR, 1H-NMR, 13C-NMR, 31P-NMR spectroscopy and elemental analysis. These polymers showed no significant weight loss below 419°C and glass transition temperatures (Tg) in the region of 231°C–290°C. The resulting polymeric films exhibited high optical transpa

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28

Holden, Catherine R., Kid Wan Shum, and David J. Gawkrodger. "Contact allergy to triphenyl phosphate: probable cross-reactivity to triphenyl phosphite present in an EN46001 System 22 clear oxygen facemask." Contact Dermatitis 54, no. 5 (2006): 299–300. http://dx.doi.org/10.1111/j.0105-1873.2006.0698d.x.

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29

Sharma, Pramod K., Divya Mathur, Shashwat Malhotra, et al. "Triphenyl Phosphite-mediated “Green” Synthesis of Novel Carboxycoumarin Amides." Current Green Chemistry 3, no. 4 (2017): 366–73. http://dx.doi.org/10.2174/2213346104666170306100140.

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30

Mei, Q., J. E. Siewenie, C. J. Benmore, P. Ghalsasi, and J. L. Yarger. "Orientational Correlations in the Glacial State of Triphenyl Phosphite." Journal of Physical Chemistry B 110, no. 20 (2006): 9747–50. http://dx.doi.org/10.1021/jp060692z.

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31

Swoboda, B., S. Buonomo, E. Leroy, and J. M. Lopez Cuesta. "Fire retardant poly(ethylene terephthalate)/polycarbonate/triphenyl phosphite blends." Polymer Degradation and Stability 93, no. 5 (2008): 910–17. http://dx.doi.org/10.1016/j.polymdegradstab.2008.02.003.

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32

Vaish, Sanjay, and Deepak Kunzru. "Triphenyl phosphite as a coke inhibitor during naphtha pyrolysis." Industrial & Engineering Chemistry Research 28, no. 9 (1989): 1293–99. http://dx.doi.org/10.1021/ie00093a005.

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33

Terashima, Y., M. Tsuchie, K. Takeda, and M. Honda. "Observation of equilibrium liquid–liquid transition in triphenyl phosphite." Chemical Physics Letters 584 (October 2013): 93–97. http://dx.doi.org/10.1016/j.cplett.2013.08.078.

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34

Beasley, M. S., B. J. Kasting, M. E. Tracy, A. Guiseppi-Elie, R. Richert, and M. D. Ediger. "Physical vapor deposition of a polyamorphic system: Triphenyl phosphite." Journal of Chemical Physics 153, no. 12 (2020): 124511. http://dx.doi.org/10.1063/5.0019872.

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35

VERONESI, B. "Biochemical and neuropathological assessment of triphenyl phosphite in rats." Toxicology and Applied Pharmacology 83, no. 2 (1986): 203–10. http://dx.doi.org/10.1016/0041-008x(86)90297-8.

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36

Yang, Chin-Ping, Huei-Wen Yang, and Ruei-Shin Chen. "Syntheses of regular copolyamides using triphenyl phosphite and pyridine." Journal of Applied Polymer Science 77, no. 1 (2000): 116–22. http://dx.doi.org/10.1002/(sici)1097-4628(20000705)77:1<116::aid-app16>3.0.co;2-m.

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37

Sobhani, Sara, and Zahra Vahidi. "P-arylation of aryl halides by an environmentally compatible method." Canadian Journal of Chemistry 95, no. 12 (2017): 1280–84. http://dx.doi.org/10.1139/cjc-2017-0364.

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In this paper, palladium–DABCO complex supported on magnetic nanoparticles was successfully used as a new magnetically recoverable heterogeneous catalyst for the synthesis of arylphosphonates via P-arylation of different types of aryl halides (aryl iodides/bromides/chlorides and benzene boronic acid/sulfonate), with phosphite esters (triethyl/triphenyl/tri-iso-propyl/diethyl/diphenyl/di-iso-propyl phosphite) in neat water without using any additive. The heterogeneous catalyst was easily isolated from the reaction mixture by an external magnet and reused five times without significant degradati

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38

Baharfar, Robabeh, and Narges Shariati. "Solvent-free Synthesis of Novel Benzothiazole-substituted 4-Thiazolidinones Using Nano Silica-bonded 5-n-Propyl-octahydro-pyrimido[1,2-a]azepinium Chloride as Catalyst." Australian Journal of Chemistry 67, no. 11 (2014): 1646. http://dx.doi.org/10.1071/ch13712.

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A series of novel benzothiazole-substituted 4-thiazolidinones were synthesised by the one-pot reaction of rhodanine-3-acetic acid derivatives, 2-aminothiophenol, and triphenyl phosphite in the presence of nano silica-bonded 5-n-propyl-octahydro-pyrimido[1,2-a]azepinium chloride (NSB-DBU) as heterogeneous reusable nanocatalyst under solvent-free conditions in high yields.

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39

Hajinasiri, Rahimeh, Zinatossadat Hossaini, Faramarz Rostami-Charati, Roghaye Mirzaie, and Sara Ahmadpoor. "Efficient Synthesis of Succinate Derivatives using Mercaptoalkanols or Mercaptophenols." Zeitschrift für Naturforschung B 67, no. 2 (2012): 154–58. http://dx.doi.org/10.1515/znb-2012-0207.

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A one-pot synthesis of dialkyl 2-(diphenoxyphosphoryl)-3-[hydroxy (alkyl)(aryl) sulfanyl] succinate derivatives via the reaction between dialkyl acetylenedicarboxylates, triphenyl phosphite and mercaptoalkanols or mercaptophenols is described. These reactions lead to the formation of dialkyl 2-(diphenoxyphosphoryl)-3-[hydroxy (alkyl)(aryl) sulfanyl] succinates as a mixture of two diastereomers without using any catalyst and in good yields.

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40

Babkov, L. M., J. Baran, N. A. Davydova, I. V. Ivlieva, E. A. Ponezha, and V. Ya Reznichenko. "Infrared Spectra of Triphenyl Phosphite and Their Interpretation on the Basis of Quantum Chemistry Calculation." Ukrainian Journal of Physics 61, no. 6 (2016): 471–77. http://dx.doi.org/10.15407/ujpe61.06.0471.

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41

Hédoux, Alain, Yannick Guinet, Marc Descamps, and Abdelkader Bénabou. "Raman Scattering Investigation of the Glaciation Process in Triphenyl Phosphite." Journal of Physical Chemistry B 104, no. 49 (2000): 11774–80. http://dx.doi.org/10.1021/jp001776p.

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42

Dvinskikh, S., G. Benini, J. Senker, et al. "Molecular Motion in the Two Amorphous Phases of Triphenyl Phosphite." Journal of Physical Chemistry B 103, no. 10 (1999): 1727–37. http://dx.doi.org/10.1021/jp983411z.

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43

Hédoux, Alain, Yannick Guinet, Patrick Derollez, Olivier Hernandez, Laurent Paccou, and Marc Descamps. "Micro-structural investigations in the glacial state of triphenyl phosphite." Journal of Non-Crystalline Solids 352, no. 42-49 (2006): 4994–5000. http://dx.doi.org/10.1016/j.jnoncrysol.2006.02.155.

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44

Lee, Dongkyu, Sungjun Koh, Da-Eun Yoon, et al. "Synthesis of InP nanocrystals using triphenyl phosphite as phosphorus source." Korean Journal of Chemical Engineering 36, no. 9 (2019): 1518–26. http://dx.doi.org/10.1007/s11814-019-0344-5.

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45

Mayer, J., J. Krawczyk, M. Massalska-Arod?, I. Natkaniec, O. Steinsvoll, and J. A. Janik. "Neutron-scattering study of low-energy excitations in triphenyl phosphite." Applied Physics A: Materials Science & Processing 74 (December 1, 2002): s439—s441. http://dx.doi.org/10.1007/s003390201646.

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46

Knoth-Anderson, Jane, Bellina Veronesi, Kim Jones, Daniel M. Lapadula, and Mohamed B. Abou-Donia. "Triphenyl phosphite-induced ultrastructural changes in bovine adrenomedullary chromaffin cells." Toxicology and Applied Pharmacology 112, no. 1 (1992): 110–19. http://dx.doi.org/10.1016/0041-008x(92)90286-2.

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47

Narva, Deshwar Kushwaha, K. Kashyap Deepak, and Srivastava Mahesh. "Microwave-assisted one pot highly efficient synthesis of 1,3-benzothiazoles and 1,3-benzoxazole." Journal of Indian Chemical Society Vol. 92, Mar 2015 (2015): 387–92. https://doi.org/10.5281/zenodo.5678758.

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Department of Chemistry, NIMS University, Shobha Nagar, Jaipur-303 121, Rajasthan, India Department of Chemistry, Meerut College, Meerut-250 001, Uttar Pradesh, India <em>E-mail </em>: narvadeshwarkushwaha@gmail.com, ashima560@gmail.com <em>Manuscript received online 07 September 2014, accepted 15 September 2014</em> Highly efficient and cost effective cyclocondensation of 2-aminothiophenols/2-aminophenols and carboxylic acids to give benzothiazoles/benzoxazoles has been reported under microwave irradiation condition using pyridine and triphenyl phosphite (TPP). The one pot methodology allowed

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48

Babkov, L. M., N. A. Davydova, and I. V. Ivlieva. "IR Spectra of Triphenyl Phosphite and Their Interpretation by Molecular Modeling." Series Physics 17, no. 1 (2017): 11–19. http://dx.doi.org/10.18500/1817-3020-2017-17-1-11-19.

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49

Kurita, Rei, Yuya Shinohara, Yoshiyuki Amemiya, and Hajime Tanaka. "Microscopic structural evolution during the liquid–liquid transition in triphenyl phosphite." Journal of Physics: Condensed Matter 19, no. 15 (2007): 152101. http://dx.doi.org/10.1088/0953-8984/19/15/152101.

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50

Deng, Zengqun, John Zhongju Zhang, Arthur B. Ellis, and Stanley H. Langer. "Catalytic Oxidation of Triphenyl Phosphite with Ferric Ion-Modified Chromatographic Silica." Journal of Liquid Chromatography 16, no. 5 (1993): 1083–103. http://dx.doi.org/10.1080/10826079308019573.

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