scholarly journals Association of Thymolsulfonephthalein and Cresolsulfonephthalein Anions with Cationic Cyanines in Aqueous Solution

2010 ◽  
Vol 4 (4) ◽  
pp. 271-276
Author(s):  
Serghiy Shapovalov ◽  
◽  
Yana Kiseliova ◽  
Keyword(s):  
Aqueous Solution ◽  
Enthalpy Of Formation ◽  
Association Constants ◽  
Semiempirical Methods ◽  
Solution Equilibrium ◽  
Spectrophotometric Data ◽  
The Enthalpy Of Formation ◽  
Quinaldine Red

The formation of associates between one- or two-charged anions of sulfonephthalein dyes – thymolsulfonephthalein, cresolsulfonephthalein – and cyanine cations (pinacyanol, quinaldine red) has been considered in aqueous solution. Equilibrium association constants have been determined using spectrophotometric data. By semiempirical methods the enthalpy of formation and the eventual structure of ions and associates have been established.

The enthalpy of formation of the praseodymium ion (3+) in an infinitely dilute aqueous solution

2006 ◽  
Vol 80 (5) ◽  
pp. 697-701
Author(s):  
Yu. V. Goryushkina ◽  
A. S. Monaenkova ◽  
A. A. Popova ◽  
L. A. Tiflova
Keyword(s):  
Aqueous Solution ◽  
Enthalpy Of Formation ◽  
Dilute Aqueous Solution ◽  
The Enthalpy Of Formation

Enantioselective Recognition of Chiral Guests by the Water-Soluble Chiral Keplerate {Mo132} Spherical Capsule with 30 Inner Lactate Ligands

2019 ◽  
Author(s):  
Nancy Watfa ◽  
Weimin Xuan ◽  
Zoe Sinclair ◽  
Robert Pow ◽  
Yousef Abul-Haija ◽  
...  
Keyword(s):  
Aqueous Solution ◽  
Chiral Recognition ◽  
Association Constants ◽  
Water Soluble ◽  
Enantioselective Recognition ◽  
H Nmr ◽  
Dosy Nmr ◽  
Spherical Capsule ◽  
Surface Pores ◽  
Guest Chemistry

Investigations of chiral host guest chemistry are important to explore recognition in confined environments. Here, by synthesizing water-soluble chiral porous nanocapsule based on the inorganic metal-oxo Keplerate-type cluster, {Mo<sub>132</sub>} with chiral lactate ligands with the composition [Mo<sub>132</sub>O<sub>372</sub>(H<sub>2</sub>O)<sub>72</sub>(<i>x-</i>Lactate)<sub>30</sub>]<sup>42-</sup> (<i>x</i> = D or L), it was possible to study the interaction with a chiral guest, L/D-carnitine and (<i>R</i>/<i>S</i>)-2-butanol in aqueous solution. The enantioselective recognition was studied by quantitative <sup>1</sup>H NMR and <sup>1</sup>H DOSY NMR which highlighted that the chiral recognition is regulated by two distinct sites. Differences in the association constants (K) of L- and D-carnitine, which, due to their charge, are generally restricted from entering the interior of the host, are observed, indicating that their recognition predominantly occurs at the surface pores of the structure. Conversely, a larger difference in association constants (K<i><sub>S</sub></i>/K<i><sub>R</sub></i> = 3) is observed for recognition within the capsule interior of (<i>R</i>)- and (<i>S</i>)-2-butanol.

Thermochemistry of Organic and Heteroorganic Species. Part IX. Photoionization Studies of Isomerization and Fragmentation of Polysubstituted Cyclopropenes: Phenyl-Substituted Cyclopropenes

2000 ◽  
Vol 6 (1) ◽  
pp. 53-64 ◽  
Author(s):  
V.V. Takhistov ◽  
I.N. Domnin ◽  
D.A. Ponomarev
Keyword(s):  
Mass Spectrometry ◽  
Enthalpy Of Formation ◽  
Good Alternative ◽  
Enthalpies Of Formation ◽  
Isodesmic Reactions ◽  
Ion Structure ◽  
Photoionization Mass Spectrometry ◽  
General Methodology ◽  
Fragment Ions ◽  
The Enthalpy Of Formation

Ionization and appearance energies of some fragment ions from 1,2,3-trimethy1-3-phenyl-, 3-methyl-1,2,3-triphenyl-, 1,2-diphenyl-3-methoxycarbonyl-, 1,2,3-triphenyl-3-methoxycarbonyl- and 1,3,3-triphenyl-2-methoxycarbonyl-cyclopropenes were measured by photoionization mass spectrometry. It was shown that in none of these compounds did the fragment ions possess the expected stable substituted cyclopropenium ion structure. Accordingly, possible schemes of molecular ion isomerization are given. The enthalpies of formation of nearly 50 substituted cyclopropenium ions, and ions of related structure, were estimated using series of isodesmic reactions. This publication, together with the previous works of the authors in this Journal, demonstrates the general methodology for estimation of the enthalpy of formation for even-electron ions. It is suggested that the present methodology can provide a good alternative to other estimation or computation procedures applied to the thermochemistry of ions.

Measurement of the enthalpy of formation of an iron pico-hydride and of its main properties

2017 ◽  
Vol 31 (25) ◽  
pp. 1745007
Author(s):  
Jacques Dufour ◽  
Xavier Dufour ◽  
Fabienne Dioury ◽  
Jenny D. Vinko
Keyword(s):  
Enthalpy Of Formation ◽  
Electric Dipole ◽  
Atomic System ◽  
Binding Energies ◽  
Iron Nucleus ◽  
Atomic Size ◽  
The Standard Model ◽  
Typical Distances ◽  
Species Being ◽  
The Enthalpy Of Formation

Chemical reactions result from the outside shell electrons of the reacting species being shared in various types of combinations. Typical distances involved are tenths of nm, resulting in binding energies typically in the order of hundreds of kJ/mole (eV/atom). The synthesis of a novel “atomic system” formed from Iron and di-Hydrogen has been achieved. The measured enthalpy of formation is some 40 MJ/moleFe and the distance between the hydrogen proton and the iron nucleus is some 8 pm, hence the proposed name: Iron Pico-Hydride. This compound is a permanent electric dipole of atomic size. Pico-Hydrides could, thus, play a significant role in HT superconductivity and in super-capacitors. The synthesis is compatible with the standard model.

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