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Journal articles on the topic 'Phosphorus trifluoride'

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1

Hillig, Kurt W., Jose Matos, Anthony Scioly, and Robert L. Kuczkowski. "The microwave spectrum of argon-phosphorus trifluoride." Chemical Physics Letters 133, no. 4 (1987): 359–62. http://dx.doi.org/10.1016/0009-2614(87)87082-3.

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2

Lascola, Robert, Robert Withnall, and Lester Andrews. "Infrared spectra of fluoroimide, nitrogen trifluoride, phosphorus trifluoride, and phosphorus trichloride and complexes with hydrogen fluoride in solid argon." Journal of Physical Chemistry 92, no. 8 (1988): 2145–49. http://dx.doi.org/10.1021/j100319a013.

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3

LaBarge, Marabeth S., Eric R. Bittner, Kurt W. Hillig, and Robert L. Kuczkowski. "The microwave spectrum and structure of krypton—phosphorus trifluoride." Journal of Molecular Structure 189, no. 1-2 (1988): 105–10. http://dx.doi.org/10.1016/0022-2860(88)80216-3.

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4

Najib, Hamid. "Experimental rovibrational constants and equilibrium structure of phosphorus trifluoride." Journal of Molecular Spectroscopy 305 (November 2014): 17–21. http://dx.doi.org/10.1016/j.jms.2014.09.008.

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5

Fowler, P. W., H. M. Kelly, and A. J. Sadlej. "Electric and magnetic properties of the phosphorus trifluoride molecule." Chemical Physics Letters 212, no. 6 (1993): 659–64. http://dx.doi.org/10.1016/0009-2614(93)85501-e.

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6

Kumar, H. P. Sampath, and D. K. Padma. "Reactions of phosphorus trifluoride and thiophosphoryl fluoride with strong oxidizing agents." Journal of Fluorine Chemistry 45, no. 1 (1989): 33. http://dx.doi.org/10.1016/s0022-1139(00)84408-5.

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7

Zhou, X. L., and J. M. White. "Coadsorption and reaction of phosphorus trifluoride with potassium on silver(111)." Journal of Physical Chemistry 95, no. 2 (1991): 887–96. http://dx.doi.org/10.1021/j100155a073.

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8

Najib, Hamid, та Hicham Msahal. "A new study of theν2(A1) infrared band of phosphorus trifluoride". Molecular Physics 109, № 15 (2011): 1953–56. http://dx.doi.org/10.1080/00268976.2011.604048.

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9

Smith, Jacob, and Richard O’Hair. "Reactions of phosphorus trifluoride with anionic nucleophiles in the gas phase." European Journal of Mass Spectrometry 2, no. 1 (1996): 225. http://dx.doi.org/10.1255/ejms.56.

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10

Hillig, Kurt W., Marabeth S. LaBarge, Amine Taleb-Bendiab, and Robert L. Kuczkowski. "The microwave spectrum and structure of the neon-phosphorus trifluoride complex." Chemical Physics Letters 171, no. 5-6 (1990): 542–46. http://dx.doi.org/10.1016/0009-2614(90)85260-j.

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11

Sampath Kumar, H. P., and D. K. Padma. "Reaction of phosphorus trifluoride and thiophosphoryl fluoride with iodine monochloride and oxidation of phosphorus trifluoride with nitryl chloride, iodic acid, periodic acid, sodium nitrite and potassium nitrite." Journal of Fluorine Chemistry 49, no. 3 (1990): 301–11. http://dx.doi.org/10.1016/s0022-1139(00)85026-5.

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12

LaBarge, Marabeth S., Anne M. Andrews, Amine Taleb-Bendiab, Kurt W. Hillig, Robert L. Kuczkowski, and Robert K. Bohn. "Microwave spectrum, structure, and dipole moment of the phosphorus trifluoride-water complex." Journal of Physical Chemistry 95, no. 9 (1991): 3523–27. http://dx.doi.org/10.1021/j100162a018.

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13

Alvey, Mark D., and John T. Yates. "Structure and chemistry of chemisorbed phosphorus trifluoride, phosphorus difluoride and phosphorus monofluoride on nickel(111): electron stimulated desorption ion angular distribution study." Journal of the American Chemical Society 110, no. 6 (1988): 1782–86. http://dx.doi.org/10.1021/ja00214a020.

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14

Jaw, Huey Rong, and Jeffrey I. Zink. "Angular-overlap interpretation of .sigma. and .pi. bonding of phosphorus trifluoride and phosphorus trichloride in platinum PtCl3L- complexes." Inorganic Chemistry 27, no. 19 (1988): 3421–24. http://dx.doi.org/10.1021/ic00292a030.

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15

KUMAR, H. P. S., and D. K. PADMA. "ChemInform Abstract: Reaction of Phosphorus Trifluoride and Thiophosphoryl Fluoride with Iodine Monochloride and Oxidation of Phosphorus Trifluoride with Nitryl Chloride, Iodic Acid, Periodic Acid, Sodium Nitrite, and Potassium Nitrite." ChemInform 22, no. 13 (2010): no. http://dx.doi.org/10.1002/chin.199113030.

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16

Wang, Xianlong, та Edward A. Wovchko. "Infrared Spectroscopic Investigation of the Surface Reaction of Phosphorus Trifluoride on γ-Alumina". Langmuir 19, № 13 (2003): 5295–302. http://dx.doi.org/10.1021/la026802k.

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17

Rodriguez, Jose A. "Adsorption of phosphorus trifluoride, hydroxyl, mercapto, and methyl on silver: a quantum-chemical study." Langmuir 7, no. 6 (1991): 1206–14. http://dx.doi.org/10.1021/la00054a031.

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18

Rodriguez, JoséA. "The adsorption of methyl, acetylide, chlorine and phosphorus trifluoride on zinc oxide: A quantum-chemical study." Surface Science 222, no. 2-3 (1989): 383–403. http://dx.doi.org/10.1016/0039-6028(89)90368-3.

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19

Rodriguez, JoséA. "The adsorption of methyl, acetylide, chlorine and phosphorus trifluoride on zinc oxide: A quantum-chemical study." Surface Science Letters 222, no. 2-3 (1989): A553. http://dx.doi.org/10.1016/0167-2584(89)90931-6.

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20

Motamedi, Masoud, and Tahere Zohrevand. "Study of Millimeter-Wave Rotational Spectra of Phosphorus Trifluoride in Ground,v2= 1 and v4= 1 States." E-Journal of Chemistry 6, no. 3 (2009): 849–65. http://dx.doi.org/10.1155/2009/458714.

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The millimeter-wave rotational spectra of the ground and excited vibrational states v2=1 and v4=1 of the symmetric top molecule, PF3, have been analyzed again. The B0= 7819.9907(13) MHz, DJ= 7.84984(41) kHz, DJk= -11.7644 (11) kHz, HJ= 15.678 (36) mHz, HJk= -66.46 (12) mHz and HkJ= 87.42 (15) mHz have been determined for ground state. The 1=±1 series have been assigned and the rotational parameters including B4=7823.09212(41) MHz, (q+t)4= -29.49200(65) MHz, rt=2.9465 (13) MHz and (Cζ)4= -3010.94684(41) MHz for v4=1 state were determined accurately
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21

Hawkins, Michael, Matthew J. Almond, and Anthony J. Downs. "Photochemistry of low-temperature matrixes containing carbonyl sulfide: reactions of sulfur atoms with the phosphorus trihalides phosphorus trifluoride (PF3) and phosphorus trichloride (PCl3) and the hydrocarbons methane, ethene, and ethyne." Journal of Physical Chemistry 89, no. 15 (1985): 3326–34. http://dx.doi.org/10.1021/j100261a034.

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22

Kohata, Hayato, and Yoji Saito. "Maskless texturization of phosphorus-diffused layers for crystalline Si solar cells by plasmaless dry etching with chlorine trifluoride gas." Solar Energy Materials and Solar Cells 94, no. 12 (2010): 2124–28. http://dx.doi.org/10.1016/j.solmat.2010.06.040.

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23

Gruetzmacher, Hansjoerg, and Hans Pritzkow. "Reaction of stannyl-substituted phosphorus ylides with boron trifluoride diethyl etherate: evidence for formation of transient triphenylphosphonio-substituted stannaethenes." Organometallics 10, no. 4 (1991): 938–46. http://dx.doi.org/10.1021/om00050a027.

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24

Song, H. "Nitrogen Trifluoride: A New Reactant Gas in Chemical Reaction Interface Mass Spectrometry for Detection of Phosphorus, Deuterium, Chlorine, and Sulfur." Journal of the American Society for Mass Spectrometry 6, no. 5 (1995): 421–27. http://dx.doi.org/10.1016/1044-0305(95)00029-d.

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25

Schmohl, Sebastian, Xuan He, and Hans-Dieter Wiemhöfer. "Boron Trifluoride Anionic Side Groups in Polyphosphazene Based Polymer Electrolyte with Enhanced Interfacial Stability in Lithium Batteries." Polymers 10, no. 12 (2018): 1350. http://dx.doi.org/10.3390/polym10121350.

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A modified polyphosphazene was synthesized using a mixed substitution at phosphorus consisting of 2-(2-methoxyethoxy)ethoxy side groups and anionic trifluoroborate groups. The primary goal was to increase the low lithium ion conductivities of the conventional lithium salt containing poly[2-(2-methoxyethoxy)ethoxy-phosphazene] (MEEP) by the immobilized anionic groups. As in previous studies, the mechanical stability was stabilized by UV induced radiation cross linking. By variation of the molar ratio between different side groups, mechanical and electrochemical properties are controllable. The polymer demonstrated large electrochemical stability windows ranging between 0 and 4.5 V versus the Li/Li+ reference. Total and lithium conductivities of 3.6 × 10−4 S·cm−1 and 1.8 × 10−5 S·cm−1 at 60 °C were revealed for the modified MEEP. When observed in special visualization cells, dendrite formation onset time and short-circuit time were determined as 21 h and 90 h, respectively, under constant current polarization (16 h and 65 h for MEEP, both with 15 wt % LiBOB), which hints to a more stable Li/polymer interface compared to normal MEEP. The enhanced dendrite suppression ability can be explained by the formation of a more conductive solid electrolyte interphase (SEI) and the existence of F-contained SEI components (such as LiF). With the addition of ethylene carbonate–dimethyl carbonate (EC/DMC) to form MEE-co-OBF3P gel polymer, both total and lithium conductivity were enhanced remarkably, and the lithium transference numbers reached reasonable values (σtotal = 1.05 mS·cm−1, σLi+ = 0.22 mS·cm−1, tLi+ = 0.18 at 60 °C).
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26

Alexander, Petr, and Antonín Holý. "General Method of Preparation of N-[(S)-(3-Hydroxy-2-phosphonomethoxypropyl)] Derivatives of Heterocyclic Bases." Collection of Czechoslovak Chemical Communications 58, no. 5 (1993): 1151–63. http://dx.doi.org/10.1135/cccc19931151.

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Reaction of (R)-1-O-p-toluenesulfonyl-1,2,3-propanetriol (IV) with N-trimethylacetylimidazole (II) afforded (R)-1-O-p-toluenesulfonyl-3-O-trimethyacetyl-1,2,3-propanetriol (V) which was reacted with dimethoxymethane in the presence of phosphorus pentoxide to give (R)-2-O-methoxymethyl-1-O-p-toluenesulfonyl-3-O-trimethyacetyl-1,2,3-propanetriol (VI). Compound VI was treated with acetic anhydride and boron trifluoride etherate and the obtained 2-acetoxy derivative VII reacted with bromotrimethylsilane to give the intermediary bromomethyl ether VIII. Compound VIII on reaction with tris(2-propyl) phosphite afforded (R)-2-O-bis(2-propyl)phosphonomethyl-1-O-p-toluenesulfonyl-3-O-trimethyacetyl-1,2,3-propanetriol (IX). Condensation of synthon IX with sodium salts of adenine, 2,6-diaminopurine, or with cytosine, 6-azacytosine or 2-chloroadenine in the presence of cesium carbonate, afforded fully protected diesters X and XIIIb which on methanolysis and reaction with bromotrimethylsilane gave N-[(S)-(3-hydroxy-2-phosphonomethoxypropyl)] derivatives of adenine (XIa), 2- chloroadenine (XIb), 2,6-diaminopurine (XIc), cytosine (XIVa) and 6-azacytosine (XIVb). In an analogous reaction, sodium salt of 4-methoxy-2-pyrimidone reacted with compound IX to give an intermediate XIIIa which on treatment with methanolic ammonia and subsequent deblocking under the same conditions also afforded the cytosine derivative XIVa. Sodium salt of 2-amino-6-chloropurine was in this way converted into the corresponding 2-aminopurine derivative XVIII. Deprotection of this compound gave 9-(S)-(3-hydroxy-2-phosphonomethoxypropyl)-2-aminopurine (XIX).
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27

Bo/rve, Knut J., and T. Darrah Thomas. "Molecular-field splitting of the 2p3/2 peak in x-ray photoelectron spectra of second-row atoms: A theoretical study of phosphine and phosphorus trifluoride." Journal of Chemical Physics 111, no. 10 (1999): 4478–86. http://dx.doi.org/10.1063/1.479211.

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28

Balch, Alan L., Brian J. Davis, and Marilyn M. Olmstead. "Complexes with a trifluorophosphine ligand bridging a tripalladium triangle. Structure of tris(.mu.-bis(diphenylphosphino)methane)(.mu.3-iodo)(.mu.3-phosphorus trifluoride)tripalladium(1+) iodide." Inorganic Chemistry 32, no. 18 (1993): 3937–42. http://dx.doi.org/10.1021/ic00070a027.

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29

Banks, R. Eric, Mohamed K. Besheesh, Suad N. Mohialdin-Khaffaf, and Iqbal Sharif. "N-Halogeno compounds part 17. Precursors of NF-TEDA reagents: quaternary salts of 1,4-diazabicyclooctane containing fluoro-anions, and their Lewis acid-Lewis base adducts with boron trifluoride, phosphorus pentafluoride and sulphur trioxide." Journal of Fluorine Chemistry 78, no. 1 (1996): 43–50. http://dx.doi.org/10.1016/0022-1139(96)03395-7.

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30

Eric Banks, R., Mohamed K. Besheesh, Suad N. Mohialdin-Khaffaf, and Iqbal Sharif. "Erratum to “N-Halogeno compounds. Part 17. Precursors of NF-TEDA reagents: quaternary salts of 1,4-diazabicyclooctane containing fluoroanions, and their Lewis acid-Lewis base adducts with boron trifluoride, phosphorus pentafluoride and sulphur trioxide”." Journal of Fluorine Chemistry 81, no. 2 (1997): 217. http://dx.doi.org/10.1016/s0022-1139(96)03537-3.

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31

Eric Banks, R., Mohamed K. Besheesh, Suad N. Mohialdin-Khaffaf, and Iqbal Sharif. "Erratum to “N-Halogeno compounds. Part 17. Precursors of NF-TEDA reagents: Quaternary salts of 1,4-diazabicyclooctane containing fluoro-anions, and their Lewis acid-Lewis base adducts with boron trifluoride, phosphorus pentafluoride and sulphur trioxide” [J. Fluorine Chemistry, 78 (1996) 43–50]." Journal of Fluorine Chemistry 82, no. 2 (1997): 193. http://dx.doi.org/10.1016/s0022-1139(96)03554-3.

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32

Jumina, Jumina. "SYNTHESIS AND REACTIONS OF 1-(4’-BROMOPHENACYL)-3-(4’-BROMO-PHENYL)-4,6-DIMETHOXYINDOLE." Indonesian Journal of Chemistry 5, no. 2 (2010): 156–62. http://dx.doi.org/10.22146/ijc.21824.

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1-Phenacyl-3-aryl-4,6-dimethoxyindoles 2b and 2c were obtained in good yields respectively through cyclization of N,N-diphenacylaniline 1b and 1c in trifluoroacetic acid. However, instead of giving pyrroloindole 3c, treatment of phenacylindole 2c with polyphosphoric acid afforded indolizine 5 in 42% yield. Phenacylindole 2c reacts with the Vilsmeier aroylation reagent consisted of a mixture of phosphoryl chloride and p-chloro-N,N-dimethylbenzamide to give 2-aroylindole 6 (32%) and pyrroloindole 7 (22%). When treated with sodium borohydride, phenacylindole 2c gave alcohol 8 in 83% yield. Nonetheless, treatment of alcohol 8 with either p-toluenesulfonic acid in glacial acetic acid or boron trifluoride etherate in benzene did not give the desired dihydropyrroloindole 12. Instead, the reactions afforded respectively acetyl ester 9 and indole 10 in 56% and 63% yield. Keywords: phenacylindole, aroylindole, pyrroloindole, and indolizine.
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33

KALBANDKERI, R. G., D. K. PADMA, and A. R. V. MURTHY. "ChemInform Abstract: REDUCTION OF PHOSPHORUS TRIFLUORIDE AND PHOSPHORYL FLUORIDE WITH LITHIUM ALUMINUM HYDRIDE." Chemischer Informationsdienst 16, no. 3 (1985). http://dx.doi.org/10.1002/chin.198503028.

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34

FRIDLAND, S. V., and M. N. MIFTAKHOV. "ChemInform Abstract: Reaction of Adducts of Phosphorus Pentachloride and Isoprene with Arsenic Trifluoride." ChemInform 19, no. 30 (1988). http://dx.doi.org/10.1002/chin.198830171.

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35

Fennema, Gary, Michelle Bates, Hayden Fox, David Gearhart, Brianne Roepke, and Kelly Murray. "Hypoxic respiratory distress potentially secondary to phosphorus trifluoride gas exposure: A case report." American Journal of Emergency Medicine, September 2021. http://dx.doi.org/10.1016/j.ajem.2021.09.018.

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36

FRIDLAND, S. V., M. N. MIFTAKHOV, and N. V. DMITRIEVA. "ChemInform Abstract: On the Reaction of Phosphorus Pentachloride 1-Alkene Adducts with Arsenic Trifluoride." Chemischer Informationsdienst 17, no. 46 (1986). http://dx.doi.org/10.1002/chin.198646281.

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37

FRIDLAND, S. V., M. N. MIFTAKHOV, and V. P. ARKHIPOV. "ChemInform Abstract: Reaction of the Adducts of Phosphorus Pentachloride and Nucleophiles Containing an Oxa Group with Arsenic Trifluoride." ChemInform 19, no. 8 (1988). http://dx.doi.org/10.1002/chin.198808275.

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38

EDWARDS, A. J., and K. I. KHALLOW. "ChemInform Abstract: THE PREPARATION AND CRYSTAL STRUCTURE OF THE 1:2 ADDUCT OF PHOSPHORUS TRIFLUORIDE OXIDE AND ANTIMONY PENTAFLUORIDE." Chemischer Informationsdienst 16, no. 6 (1985). http://dx.doi.org/10.1002/chin.198506006.

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39

FRIDLAND, S. V., M. N. MIFTAKHOV, N. V. DMITRIEVA, and V. P. ARKHIPOV. "ChemInform Abstract: Reaction of Phosphorus Pentachloride with 2-Chloroheptylphosphonic Dichloride in Benzene and Subsequent Treatment of the Reaction Mixture with Arsenic Trifluoride." ChemInform 19, no. 6 (1988). http://dx.doi.org/10.1002/chin.198806233.

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40

HADDAD, M., M. T. BOISDON, L. LOPEZ, et al. "ChemInform Abstract: Dicoordinated Phosphorus Compounds: 13C and 15N NMR Study of 1,2,4,3-Triazaphospholes Disubstituted at the 1,5- and 2,5-Positions. Structure of the Complex 5-Benzyl-2-methyl-1,2,4,3-triazaphosphole-Boron Trifluoride." ChemInform 21, no. 1 (1990). http://dx.doi.org/10.1002/chin.199001051.

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41

Gonay, Marie, Chloé Batisse, and Jean-François Paquin. "Recent Advances in the Synthesis of Acyl Fluorides." Synthesis, October 27, 2020. http://dx.doi.org/10.1055/s-0040-1705951.

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AbstractAcyl fluorides are valuable intermediates in organic synthesis. They are increasingly employed in peptide synthesis, in challenging esterification and amidation reactions or in transition-metal-catalyzed transformations. This review summarizes recent advances in their preparation.1 Introduction2 Nucleophilic Fluorination2.1 α-Fluoroamine Reagents2.2 Sulfur-Based Reagents2.3 Metal Catalysts2.4 Phosphorus-Based Reagents2.5 N,N′-Dicyclohexylcarbodiimide/HF·Pyridine2.6 Uranium Hexafluoride2.7 Bromine Trifluoride3 Radical Fluorination4 Conclusion
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