Relevant bibliographies by topics / Triaminocyclopropenium

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Triaminocyclopropenium'

Author: Grafiati
Published: 4 June 2021
Last updated: 8 February 2022

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Journal articles on the topic "Triaminocyclopropenium"

1

Curnow, Owen J., Douglas R. MacFarlane, and Kelvin J. Walst. "Triaminocyclopropenium salts as ionic liquids." Chemical Communications 47, no. 37 (2011): 10248. http://dx.doi.org/10.1039/c1cc13979g.

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2

Curnow, Owen J., and Ruhamah Yunis. "Synthesis, characterization and properties of amino acid ionic liquids derived from the triaminocyclopropenium cation." RSC Advances 6, no. 74 (2016): 70152–64. http://dx.doi.org/10.1039/c6ra10171b.

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3

Walst, Kelvin J., Ruhamah Yunis, Paul M. Bayley, et al. "Synthesis and physical properties of tris(dialkylamino)cyclopropenium bistriflamide ionic liquids." RSC Advances 5, no. 49 (2015): 39565–79. http://dx.doi.org/10.1039/c5ra05254h.

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An investigation of symmetry (D<sub>3h</sub>, C<sub>3h</sub>, C<sub>2v</sub> and C<sub>s</sub>) and alkyl chain length (6–60 alkyl carbon atoms) effects on the physical properties of peralkylated triaminocyclopropenium bistriflamide salts.
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4

Curnow, Owen J., Matthew I. J. Polson, Kelvin J. Walst, and Ruhamah Yunis. "Synthesis and physical properties of tris(dialkylamino)cyclopropenium dicyanamide ionic liquids." RSC Advances 8, no. 50 (2018): 28313–22. http://dx.doi.org/10.1039/c8ra05558k.

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An investigation of symmetry (D<sub>3h</sub>, C<sub>3h</sub>, C<sub>2v</sub> and C<sub>s</sub>) and alkyl chain length (6–60 alkyl carbon atoms) effects on the physical properties of peralkylated triaminocyclopropenium dicyanamide salts.
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5

Curnow, Owen J., Kelvin J. Walst, and Ruhamah Yunis. "Synthesis and Physical Properties of Protic Triaminocyclopropenium Ionic Liquids." ChemistrySelect 5, no. 23 (2020): 6978–86. http://dx.doi.org/10.1002/slct.202000609.

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6

Curnow, Owen J., Chaminda D. Jayasinghe, Matthew I. J. Polson, and Ruhamah Yunis. "Triaminocyclopropenium Halide and Triiodide Salts: The Formation of Cyclopropenium Dimers." Journal of Chemical Crystallography 50, no. 4 (2019): 357–72. http://dx.doi.org/10.1007/s10870-019-00809-1.

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7

Jin, Yunhe, Binshen Wang, Wenquan Zhang, et al. "Synthesis and Properties of Triaminocyclopropenium Cation Based Ionic Liquids as Hypergolic Fluids." Chemistry – A European Journal 24, no. 18 (2018): 4620–27. http://dx.doi.org/10.1002/chem.201705506.

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8

Curnow, Owen J., Michael T. Holmes, Leonardus C. Ratten, Kelvin J. Walst, and Ruhamah Yunis. "A facile route to functionalised, protic and chiral ionic liquids based on the triaminocyclopropenium cation." RSC Advances 2, no. 29 (2012): 10794. http://dx.doi.org/10.1039/c2ra22078d.

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Dissertations / Theses on the topic "Triaminocyclopropenium"

1

Walst, Kelvin John. "Synthesis and Characterization of Triaminocyclopropenium Ionic Liquids." Thesis, University of Canterbury. Chemistry, 2013. http://hdl.handle.net/10092/7637.

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This thesis describes the synthesis and characterization of triaminocyclopropenium, [C3(NR2)3]+, ionic liquids. A range of triaminocyclopropenium salts were prepared: D3h, C3h, C2v and Cs symmetric cations with a variety of substituents. D3h and C3h symmetric cations were prepared from pentachlorocyclopropane and dialkylamines, whereas a variety of methods were investigated for C2v and Cs symmetric cations, with the most versatile synthesis involving the alkylation of bis(dialkylamino)cyclopropenone followed by reaction with dialkylamine. Metathesis with a range of common ionic liquid anions w
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2

Yunis, Ruhamah. "Synthesis and characterization of amino acid ionic liquids and low symmetry ionic liquids based on the triaminocyclopropenium cation." Thesis, University of Canterbury. Chemistry, 2015. http://hdl.handle.net/10092/10207.

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This thesis involves the synthesis of two main classes of triaminocyclopropenium (tac) Ionic Liquids (ILs) (i) Amino Acid Ionic Liquids (AAILs) and (ii) reduced-symmetry cations. [C₃(NEt₂)₂(NRR’)]X (X = TFSA and MeSO₄) were prepared, whereby NHR is derived from amino acids. Optically pure AAILs, [E₄AminoAcid]X (X = TFSA and MeSO₄) were obtained as a mixture of the IL and its zwitterion. The ratios of these mixtures were determined by pH titration and microanalysis. The AAILs specific rotations and pKa values were determined. AAILs can be used for chiral discrimination and form diasterreomeric
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