Journal articles on the topic 'Trifluoroacetate'

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1

Gleghorn, J. T., and R. W. H. Small. "The trifluoroacetato (and trifluoroacetate) group, CF3COO-(TFA)." Acta Crystallographica Section A Foundations of Crystallography 49, s1 (August 21, 1993): c239. http://dx.doi.org/10.1107/s0108767378093368.

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2

Mirny, V. N., V. V. Trachevski, and T. A. Mimaya. "Nuclear Magnetic Resonance Study of Caesium-133 in Binary Molten Trifluoroacetate Salt Mixtures." Zeitschrift für Naturforschung A 56, no. 3-4 (April 1, 2001): 288–90. http://dx.doi.org/10.1515/zna-2001-0310.

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Abstract The chemical shifts of Cs+ in binary melts of caesium trifluoroacetate with lithium, sodium, potassium or thallium trifluoroacetates have been studied as a function of composition. An influence of added foreign cations on chemical shift of caesium nuclei has been found. The nature of the intra-and intermolecular paramagnetic contributions into the shifts of 133Cs is discussed.
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3

Smrčková, Svatava, Kristina Juricová, and Viktor Prutianov. "Study of Amino-Imino Tautomerism in Derivatives of 2-, 4- and 6-Aminonicotinic Acid." Collection of Czechoslovak Chemical Communications 59, no. 9 (1994): 2057–68. http://dx.doi.org/10.1135/cccc19942057.

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13C NMR spectra of p-nitrobenzoyl 2-, 4-, and 6-aminopyridine-3-carboxylates, their hydrochlorides, trifluoroacetates and 1-benzyl derivatives were studied. As found from the chemical shifts of pyridine carbon atoms C-2, C-4 and C-6, the free bases exist in the amino form whereas hydrochlorides and 1-substituted pyridinium derivatives in the imino form. Trifluoroacetates of the 2- and 6-amino derivatives have structure similar to that of amidiniumcarboxylates (parallel hydrogen bonds and partially ionic character) whereas trifluoroacetate of the 4-amino derivative is structurally close to the corresponding hydrochloride. The found structures were confirmed by 1H NMR and IR spectroscopy.
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4

Hietsoi, Oleksandr, Alexander S. Filatov, and Marina A. Petrukhina. "Building a two-dimensional network from mixed-valence copper units held together by acetone bridges." Acta Crystallographica Section C Crystal Structure Communications 69, no. 12 (November 8, 2013): 1416–20. http://dx.doi.org/10.1107/s0108270113025559.

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The mixed-valence supramolecular product di-μ2-acetone-di-μ3-trifluoroacetato-deca-μ2-trifluoroacetato-octacopper(I)dicopper(II), [Cu10(C2F3O2)12(C3H6O)2] or {[CuI4(O2CCF3)4]2–{μ2-OC(CH3)2}2–[CuII2(O2CCF3)4]}, was prepared by co-deposition of two building units, namely a bis-acetone adduct of [CuII2(O2CCF3)4] and a very electrophilic tetranuclear [CuI4(O2CCF3)4] complex. The asymmetric unit contains one molecule of the compound with a total of ten independent Cu atoms. Acetone molecules serve as bridges between the [CuII2(O2CCF3)4] and [CuI4(O2CCF3)4] units. Additionally, the tetracopper(I) trifluoroacetate units are involved in intermolecular Cu...O interactions, forming a layered two-dimensional network in the extended structure.
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5

Ng, S. W., H. K. Fun, and S. Shanmuga Sundara Raj. "Dicyclohexylammonium trifluoroacetate." Acta Crystallographica Section C Crystal Structure Communications 55, no. 12 (December 15, 1999): 2145–47. http://dx.doi.org/10.1107/s0108270199010999.

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6

Rodrigues, V. H., J. A. Paixão, M. M. R. R. Costa, and A. Matos Beja. "Glycinium trifluoroacetate." Acta Crystallographica Section C Crystal Structure Communications 58, no. 11 (October 22, 2002): o658—o660. http://dx.doi.org/10.1107/s010827010201778x.

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7

Frank, Hartmut, Armin Klein, and Dirk Renschen. "Environmental Trifluoroacetate." Nature 382, no. 6586 (July 1996): 34. http://dx.doi.org/10.1038/382034a0.

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8

Athimoolam, S., and S. Natarajan. "Nicotinium trifluoroacetate." Acta Crystallographica Section E Structure Reports Online 63, no. 5 (April 25, 2007): o2656. http://dx.doi.org/10.1107/s1600536807019216.

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9

Rodrigues, V. H., J. A. Paixão, M. M. R. R. Costa, and A. Matos Beja. "Betainium trifluoroacetate." Acta Crystallographica Section C Crystal Structure Communications 57, no. 6 (June 12, 2001): 761–63. http://dx.doi.org/10.1107/s0108270101004966.

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10

Rodrigues, V. H., J. A. Paixão, M. M. R. R. Costa, and A. Matos Beja. "Sarcosinium trifluoroacetate." Acta Crystallographica Section C Crystal Structure Communications 56, no. 8 (August 1, 2000): 1053–55. http://dx.doi.org/10.1107/s010827010000809x.

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11

Suresh, J., R. V. Krishnakumar, and S. Natarajan. "L-Argininium trifluoroacetate." Acta Crystallographica Section E Structure Reports Online 62, no. 7 (June 30, 2006): o3127—o3129. http://dx.doi.org/10.1107/s1600536806024743.

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In the title compound, C6H16N4O2 +·C2F3O2 −, the amino acid exists as a zwitterionic argininium cation, with positively charged amino and guanidinium groups and a negatively charged carboxylate group. The trifluoroacetic acid molecule is deprotonated. The stoichiometry between the argininium ion and the trifluoroacetate anion is 1:1. The aggregation of argininium cations and trifluoroacetate anions is strikingly similar to those observed in the 1:2 stoichiometric analogue.
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12

Petrosyan, A. M., V. V. Ghazaryan, G. Giester, and M. Fleck. "Sarcosine sarcosinium trifluoroacetate." Journal of Molecular Structure 1115 (July 2016): 117–23. http://dx.doi.org/10.1016/j.molstruc.2016.02.094.

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13

Paixão, J. A., P. S. Pereira Silva, A. Matos Beja, M. Ramos Silva, and L. Alte da Veiga. "1,3-Diphenylguanidinium Trifluoroacetate." Acta Crystallographica Section C Crystal Structure Communications 54, no. 10 (October 15, 1998): 1484–86. http://dx.doi.org/10.1107/s0108270198005095.

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14

Suresh, J., and S. Natarajan. "DL-Valinium trifluoroacetate." Acta Crystallographica Section E Structure Reports Online 62, no. 8 (July 14, 2006): o3331—o3333. http://dx.doi.org/10.1107/s1600536806026638.

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15

Sun, Zhi Hua, Jian Dong Fan, Guang Hui Zhang, Xin Qiang Wang, and Dong Xu. "L-Lysinium trifluoroacetate." Acta Crystallographica Section E Structure Reports Online 64, no. 2 (January 9, 2008): o393—o394. http://dx.doi.org/10.1107/s1600536807068791.

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16

Hemamalini, Madhukar, and Hoong-Kun Fun. "2-Aminopyridinium trifluoroacetate." Acta Crystallographica Section E Structure Reports Online 66, no. 3 (February 27, 2010): o691—o692. http://dx.doi.org/10.1107/s1600536810006392.

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17

Gokul Raj, Srinivasan, Gubendiran Ramesh Kumar, Rajagopal Mohan, and Ramasamy Jayavel. "L-Histidinium trifluoroacetate." Acta Crystallographica Section E Structure Reports Online 62, no. 1 (December 3, 2005): o5—o7. http://dx.doi.org/10.1107/s1600536805038791.

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18

Gol'dshleger, N. F., A. P. Moravskii, and Yu M. Shul'ga. "Rhodium(III) trifluoroacetate." Bulletin of the Academy of Sciences of the USSR Division of Chemical Science 40, no. 1 (January 1991): 238. http://dx.doi.org/10.1007/bf00959682.

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19

Sekiguchi, Osamu, Sou Tajima, Risei Koitabashi, and Susumu Tajima. "Decomposition of metastable methyl trifluoroacetate and ethyl trifluoroacetate upon electron impact." International Journal of Mass Spectrometry 177, no. 1 (August 1998): 23–30. http://dx.doi.org/10.1016/s1387-3806(98)14011-3.

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20

Wheaton, Craig A., Michael C. Jennings, and Richard J. Puddephatt. "Complexes of Gold(I) with a Chiral Diphosphine Ligand: A Polymer with Both Au···Ag and Ag···Ag Metallophilic Bonds." Zeitschrift für Naturforschung B 64, no. 11-12 (December 1, 2009): 1469–77. http://dx.doi.org/10.1515/znb-2009-11-1230.

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The chemistry of gold(I) with the ligand binap = 2,2'-bis(diphenylphosphino)-1,1' -binaphthyl is reported. Reaction of [Au2Cl2(μ-binap)] with silver trifluoroacetate gave the corresponding complex [Au2(O2CCF3)2(μ-binap)], and crystallization in the presence of excess silver trifluoroacetate gave the unusual syndiotactic polymeric complex [{Au2Ag2(μ-O2CCF3)4(μ-binap)}n], which contains both Au・ ・ ・Ag and Ag・ ・ ・Ag metallophilic bonds. The trifluoroacetate ligands in [Au2(O2CCF3)2(μ- binap)] can be replaced by nitrogen or phosphorus donor ligands to give complexes [Au2(κ1-4,4'- bipyridine)2(μ-binap)](CF3CO2)2 or meso-[Au2(μ-binap)2](CF3CO2)2
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21

Silva, Manuela Ramos, José A. Paixão, and Ana Matos Beja. "L-Argininium bis(trifluoroacetate)." Acta Crystallographica Section E Structure Reports Online 59, no. 12 (November 8, 2003): o1912—o1914. http://dx.doi.org/10.1107/s1600536803025169.

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22

Frank, Hartmut, Eugen H. Christoph, Osmund Holm-Hansen, and John L. Bullister. "Trifluoroacetate in Ocean Waters." Environmental Science & Technology 36, no. 1 (January 2002): 12–15. http://dx.doi.org/10.1021/es0101532.

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23

Richey, D. G., C. T. Driscoll, and G. E. Likens. "Soil Retention of Trifluoroacetate." Environmental Science & Technology 31, no. 6 (June 1997): 1723–27. http://dx.doi.org/10.1021/es960649x.

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24

Liu, Ming-Liang. "Tris(hydroxymethyl)methanaminium trifluoroacetate." Acta Crystallographica Section E Structure Reports Online 68, no. 1 (December 10, 2011): o60. http://dx.doi.org/10.1107/s1600536811052226.

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25

Athimoolam, S., and S. Natarajan. "3-(Aminocarbonyl)pyridinium trifluoroacetate." Acta Crystallographica Section E Structure Reports Online 63, no. 5 (April 18, 2007): o2430—o2432. http://dx.doi.org/10.1107/s1600536807015310.

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26

Hernández Linares, María-Guadalupe, Gabriel Guerrero Luna, and Sylvain Bernès. "(R)-1-Phenylethylammonium trifluoroacetate." Acta Crystallographica Section E Structure Reports Online 66, no. 5 (April 21, 2010): o1118. http://dx.doi.org/10.1107/s1600536810013565.

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27

Salvanna, N., Biswanath Das, and P. Reddy. "Palladium-Catalyzed Cross-Coupling of 1,3,4-Oxadiazoles and Styrenes: An Efficient Method to Synthesize 2-Alkenyl-1,3,4- Oxadiazoles§." Synlett 29, no. 01 (August 25, 2017): 71–74. http://dx.doi.org/10.1055/s-0036-1588561.

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2-Alkenyl-1,3,4-oxadiazole derivatives have been prepared by cross-coupling of 1,3,4-oxadiazoles with styrenes by using palladium(II) trifluoroacetate [Pd(TFA)2] as a catalyst, 1,10-phenanthroline as a ligand, silver trifluoroacetate as an oxidant, and toluene as a solvent. The products were formed in high yields and no byproducts were detected.
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28

Hu, Xiaomei, Bixian Zhang, Shijia Dong, and Yunfei Gao. "Modification of Thionucleobases in Ionic Liquids." Journal of Chemistry 2014 (2014): 1–4. http://dx.doi.org/10.1155/2014/353797.

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A simple method was established for the preparation of thio-substituted thionucleobases using room temperature ionic liquids (RTILs) such as 1-butyl-3-methylimidazolium trifluoroacetate [BMIM]+[CF3COO]−and 1-methoxyethyl-3-methylimidazolium trifluoroacetate [MeOEtMIM]+[CF3COO]−as solvents and catalysts without any other catalyst. These reactions proceeded efficiently in RTILs with excellent yield of products. RTILs can be recycled and reused effectively without further purification.
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29

Cambie, RC, PA Craw, DK Murray, PS Rutledge, PA Schwerdtfeger, M. Seth, and PD Woodgate. "Dimers of Podocarpic Acid Derivatives." Australian Journal of Chemistry 49, no. 1 (1996): 167. http://dx.doi.org/10.1071/ch9960167.

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Treatment of methyl 12-hydroxypodocarpa-8,11,13-trien-19-oate (5) with a commercial sample of thallium(III) trifluoroacetate gave a low yield (5%) of a non-symmetric ether-linked dimer (15). Use of freshly prepared thallium(III) trifluoroacetate gave a 28% yield of the symmetrical biaryl dimer (16). The dimethyl ether (17) was prepared in low yield (10%) by treatment of methyl 12-methoxypodocarpa-8,11,13-trien-19-oate (4) with the latter reagent.
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30

Cambie, RC, PI Higgs, CM Read, PS Rutledge, GR Ryan, and PD Woodgate. "Phenolic Oxidations of Totarol." Australian Journal of Chemistry 43, no. 4 (1990): 681. http://dx.doi.org/10.1071/ch9900681.

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Methods for the direct oxidation of the C12 position of totarol (1) or its methyl ether (4) have been examined. Treatment of (1) with benzeneseleninic anhydride gave the 9-hydroxy dienone (16) which on ozonolysis afforded the spiro butenolide (21), formed via the ozonide (22). The rearranged ether (18) was obtained from one oxidation with benzeneseleninic anhydride. Mercuriation of totarol and totaryl methyl ether gave the mercuriochlorides (5) and (7) but attempts to form the methoxy acetate (6) from (7) by boronation /oxidation and acetylation were unsuccessful. Treatment of totaryl methyl ether (4) with thallium(III) trifluoroacetate gave dienone 14- and 9-trifluoroacetates (25) and (17). Reaction of the (η6-arene) tricarbonylchromium(0) complexes (28) and (29) of (4) with lithioacetonitrile gave the 7α-alcohol (30) but reaction with t- butyllithium and then with copper(I) bromide/ dimethyl sulfide and MoOPH gave the methoxyphenol (12) in 66% yield.
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31

Suggs, J. William, and Larry Ytuarte. "Hydrocarbon oxidations with chromyl trifluoroacetate." Tetrahedron Letters 27, no. 4 (January 1986): 437–40. http://dx.doi.org/10.1016/s0040-4039(00)85499-4.

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32

Thanigaimani, Kaliyaperumal, Abbas Farhadikoutenaei, Nuridayanti Che Khalib, Suhana Arshad, and Ibrahim Abdul Razak. "2-Amino-5-methylpyridinium trifluoroacetate." Acta Crystallographica Section E Structure Reports Online 68, no. 12 (November 10, 2012): o3319—o3320. http://dx.doi.org/10.1107/s1600536812045291.

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33

Breitung, Sven, Hans-Wolfram Lerner, and Michael Bolte. "2,2,6,6-Tetramethyl-4-oxopiperidinium trifluoroacetate." Acta Crystallographica Section E Structure Reports Online 59, no. 4 (March 14, 2003): o445—o446. http://dx.doi.org/10.1107/s1600536803004938.

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34

Jovita, Josephine Viavulamary, Shanmugam Sathya, Govindasamy Usha, Ramachandran Vasanthi, and Krishnan Sarada Ezhilarasi. "2-Amino-5-nitropyridinium trifluoroacetate." Acta Crystallographica Section E Structure Reports Online 69, no. 6 (May 11, 2013): o841—o842. http://dx.doi.org/10.1107/s1600536813011896.

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35

Li, Jiang-Sheng, Mei-Lian Fan, Wen-Sheng Li, and Wei-Dong Liu. "4-(2-Nitrobenzenesulfonamido)pyridinium trifluoroacetate." Acta Crystallographica Section E Structure Reports Online 64, no. 8 (July 12, 2008): o1459. http://dx.doi.org/10.1107/s1600536808020825.

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36

Li, Jiang-Sheng, Mei-Lian Fan, Wen-Sheng Li, and Wei-Dong Liu. "4-(4-Nitrobenzenesulfonamido)pyridinium trifluoroacetate." Acta Crystallographica Section E Structure Reports Online 64, no. 8 (July 16, 2008): o1513. http://dx.doi.org/10.1107/s1600536808021405.

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37

Pohnert, Georg. "Phenyliodine(III) bis(trifluoroacetate) (PIFA)." Journal für praktische Chemie 342, no. 7 (September 2000): 731–34. http://dx.doi.org/10.1002/1521-3897(200009)342:7<731::aid-prac731>3.0.co;2-e.

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38

Pereira Silva, P. S., C. Cardoso, M. Ramos Silva, and J. A. Paixão. "N,N′,N′′-Triphenylguanidinium trifluoroacetate." Acta Crystallographica Section E Structure Reports Online 63, no. 2 (January 10, 2007): o501—o503. http://dx.doi.org/10.1107/s1600536806055899.

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39

Chen, Yan-Xue, Mei-Ling Han, Yi Deng, and Jin-Hui Yang. "4-Hydroxy-2,2,6,6-tetramethylpiperidinium trifluoroacetate." Acta Crystallographica Section E Structure Reports Online 64, no. 1 (December 18, 2007): o275. http://dx.doi.org/10.1107/s1600536807066305.

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40

Hemamalini, Madhukar, and Hoong-Kun Fun. "2-Amino-5-bromopyridinium trifluoroacetate." Acta Crystallographica Section E Structure Reports Online 66, no. 4 (March 6, 2010): o775. http://dx.doi.org/10.1107/s1600536810008184.

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41

Hemamalini, Madhukar, and Hoong-Kun Fun. "2-Amino-5-chloropyridinium trifluoroacetate." Acta Crystallographica Section E Structure Reports Online 66, no. 4 (March 10, 2010): o783—o784. http://dx.doi.org/10.1107/s1600536810008196.

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42

Hemamalini, Madhukar, and Hoong-Kun Fun. "2-Amino-4-methylpyridinium trifluoroacetate." Acta Crystallographica Section E Structure Reports Online 66, no. 4 (March 10, 2010): o781—o782. http://dx.doi.org/10.1107/s1600536810008202.

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43

Singh, Dharmendra, Vickramjeet Singh, Nasarul Islam, and Ramesh L. Gardas. "Elucidation of molecular interactions between a DBU based protic ionic liquid and organic solvents: thermophysical and computational studies." RSC Advances 6, no. 1 (2016): 623–31. http://dx.doi.org/10.1039/c5ra18843a.

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44

Manabe, T., I. Yamaguchi, W. Kondo, T. Kumagai, and S. Mizuta. "Low temperature solid-state epitaxy of LiNbO3 films by a dipping-pyrolysis process using Li-trifluoroacetate." Journal of Materials Research 13, no. 4 (April 1998): 834–36. http://dx.doi.org/10.1557/jmr.1998.0108.

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Epitaxially grown LiNbO3 thin films were prepared on sapphire(012) (R-plane) substrates by a dipping-pyrolysis process using two kinds of lithium sources, i.e., Li-2-ethylhexanoate and Li-trifluoroacetate, which are pyrolyzed in air to Li2CO3 and LiF, respectively. Crystallization temperature and alignment of LiNbO3 films on sapphire(012) were found to depend greatly on the Li sources. Dominantly [100]-oriented epitaxial LiNbO3 films were crystallized at around 600 °C using 2-ethylhexanoate, whereas dominantly [012]-oriented epitaxial LiNbO3 films resulted at a temperature as low as 400 °C using trifluoroacetate.
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45

Lo, Kong Mun, and Seik Weng Ng. "Diaqua(trifluoroacetato-κ2O,O′)[2,4,6-tri-2-pyridyl-1,3,5-triazine-κ3N2,N1,N6]manganese(II) trifluoroacetate." Acta Crystallographica Section E Structure Reports Online 65, no. 5 (April 30, 2009): m591—m592. http://dx.doi.org/10.1107/s1600536809015098.

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46

Kaipara, Revathy, and B. Rajakumar. "Cl Atom-Initiated Photo-Oxidation Reactions of Vinyl Trifluoroacetate and Allyl Trifluoroacetate in Tropospheric Conditions." Journal of Physical Chemistry A 124, no. 11 (February 25, 2020): 2123–39. http://dx.doi.org/10.1021/acs.jpca.9b11166.

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47

Li, Rongrong, Zehua Zhou, Jingjing Chen, Shiting Wang, Jianli Zheng, Chu Chu, Jia Zhao, Huajun Fan, and Deman Han. "The improved hydrodechlorination catalytic reactions by concerted efforts of ionic liquid and activated carbon support." New Journal of Chemistry 43, no. 17 (2019): 6659–65. http://dx.doi.org/10.1039/c9nj00273a.

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48

Silva, O. Fernando, Rita H. de Rossi, and N. Mariano Correa. "The hydrolysis of phenyl trifluoroacetate in AOT/n-heptane RMs as a sensor of the encapsulated water structure." RSC Advances 5, no. 44 (2015): 34878–84. http://dx.doi.org/10.1039/c5ra03532e.

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49

Cotton, F. Albert, Evgeny V. Dikarev, Marina A. Petrukhina, and Salah-Eddine Stiriba. "Studies of dirhodium(II) tetrakis(trifluoroacetate)." Polyhedron 19, no. 15 (July 2000): 1829–35. http://dx.doi.org/10.1016/s0277-5387(00)00472-1.

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50

Farjas, J., J. Camps, P. Roura, S. Ricart, T. Puig, and X. Obradors. "The thermal decomposition of barium trifluoroacetate." Thermochimica Acta 544 (September 2012): 77–83. http://dx.doi.org/10.1016/j.tca.2012.06.020.

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