The heats of combustion of some organic bases and their salts. The resonance energies of acridine and phenazine

1947 ◽  
Vol 43 ◽  
pp. 97 ◽  
Author(s):  
J. B. Willis
Keyword(s):  
Organic Bases ◽  
Resonance Energies ◽  
Heats Of Combustion

scholarly journals The Heats of Combustion and Formation of the Three Diazines and their Resonance Energies.

1962 ◽  
Vol 16 ◽  
pp. 916-921 ◽  
Author(s):  
Jan Tjebbes ◽  
René Mollberg ◽  
Bengt Lindberg ◽  
James McKay ◽  
Olof Theander ◽  
...  
Keyword(s):  
Resonance Energies ◽  
Heats Of Combustion

Cytochemical analysis of mast cell granules after poly-dl-lysine action

1978 ◽  
Vol 36 (2) ◽  
pp. 278-279
Author(s):  
R. Courtoy ◽  
L.J. Simar ◽  
J. Christophe
Keyword(s):  
Mast Cell ◽  
Mast Cells ◽  
Chemical Compounds ◽  
Cellular Membrane ◽  
Thin Sections ◽  
Organic Bases ◽  
Ferric Thiocyanate ◽  
Cytochemical Analysis ◽  
Mast Cell Granule ◽  
Amine Liberation

Several chemical compounds induce amine liberation from mast cells but do not necessarily provoque the granule expulsion. For example, poly-dl-lysine induces modifications of the cellular membrane permeability which promotes ion exchange at the level of mast cell granules. Few of them are expulsed but the majority remains in the cytoplasm and appears less dense to the electrons. A cytochemical analysis has been performed to determine the composition of these granules after the polylysine action.We have previously reported that it was possible to demonstrate polyanions on epon thin sections using a cetylpyridinium ferric thiocyanate method. Organic bases are selectively stained with cobalt thiocyanate and the sulfhydryle groups are characterized with a silver methenamine reaction. These techniques permit to reveal the mast cell granule constituents, i.e. heparin, biogenic amines and basic proteins.

Reactivity of Montmorillonite Surfaces with Weak Organic Bases

1969 ◽  
Vol 33 (5) ◽  
pp. 818-818 ◽  
Author(s):  
M. M. Mortland ◽  
V. C. Farmer ◽  
J. D. Russell
Keyword(s):  
Organic Bases

New type of addition to 5-substituted 4-arylidene-2-(4,5-dihydrofurfurylidene)-N,N-dimethyliminium bisperchlorates. Preparation of 4-substituted 5-(N,N-dimethylamino)-2-furancarbaldehydes

1986 ◽  
Vol 51 (3) ◽  
pp. 573-580 ◽  
Author(s):  
Tibor Gracza ◽  
Zdeněk Arnold ◽  
Jaroslav Kováč
Keyword(s):  
Nmr Spectra ◽  
Addition Reaction ◽  
H Nmr ◽  
Organic Bases ◽  
New Type

4-Arilidene-5-(N,N-dimethyliminium)-2-(4,5-dihydrofurfurylidene)-N,N-dimethyliminium bisperchlorate I undergoes a 1,4-addition reaction with organic bases under re-formation of the furan nucleus; this behaviour has been utilized in the preparation of new 4-substituted 5-(N,N-dimethylamino)-2-furancarbaldehydes II, III. The structure of the prepared compounds has been confirmed by 13C and 1H NMR spectra.

Aromaticity in heterocyclic molecules containing divalent sulfur

1988 ◽  
Vol 53 (9) ◽  
pp. 2023-2054 ◽  
Author(s):  
Milan Randić ◽  
Sonja Nikolić ◽  
Nenad Trinajstić
Keyword(s):  
Sulfur Atom ◽  
Positional Isomers ◽  
Heterocyclic Molecules ◽  
Resonance Energies ◽  
Conjugated Circuits ◽  
Divalent Sulfur

The conjugated circuits model is applied to heterocycles containing divalent sulfur. A novel parametrization is introduced for 4n + 2 and 4n conjugated circuits containing a single sulfur atom. The relative aromatic stabilities of a number of heterocyclic systems containing divalent sulfur are studied. Comparison is made whenever possible with earlier reported resonance energies of these compounds, obtained by using Huckel MO and SCF π-MO models, and appropriate reference structures. Special attention is given to positional isomers. An explanation of the differences amongst such isomers is given.

Examination of the Conditions of Extraction of Toxic Organic Bases and of Methods of Their Determination. III. Extraction of Ion-Associates of Dibenz[b,f]-1,4-oxazepin

1994 ◽  
Vol 59 (3) ◽  
pp. 582-588
Author(s):  
Jan Souček ◽  
Ladislav Belický ◽  
Josef Havel
Keyword(s):  
Aqueous Phase ◽  
Basic Dye ◽  
Organic Bases ◽  
Safranine T ◽  
Extraction Constants ◽  
Distribution Constants

The protonation and distribution constants of dibenz[b, f]-1,4-oxazepin (CR) were measured. This substance forms stable ion-associates with Acid Red 88, extractable into chloroform. Reextraction with an aqueous phase containing basic fuchsine or safranine T brings about exchange of the CR cation for the basic dye cation. The associates so formed exhibit higher conditional extraction constants and higher molar absorptivities than the initial associates.

Determination of Organic Bases by Ion-Pair Extraction Polarography Using Orange II as Counter Ion

1992 ◽  
Vol 57 (11) ◽  
pp. 2272-2278 ◽  
Author(s):  
Václav Koula ◽  
Daria Kučová ◽  
Jiří Gasparič
Keyword(s):  
Model Compound ◽  
Differential Pulse ◽  
Ion Pair ◽  
Differential Pulse Polarography ◽  
Orange Ii ◽  
Organic Bases ◽  
Counter Ion ◽  
Pulse Polarography ◽  
Ammonium Compounds

The combination of ion-pair extraction and differential pulse polarography is shown to be a method suitable for the determination of 10-7 mol l-1 concentrations of organic bases of quaternary ammonium compounds. Orange II (4-[2-hydroxy-1-naphtyl]azobenzenesulfonic acid) was found to be an appropriate polarographically active counter-ion. The proposed method was used for the determination of tetrapentylammonium bromide (as model compound), Septonex ([1-(ethoxycarbonyl)-pentadecyl]trimethylammonium bromide) and codeine.

(p, γ) Resonance-Curve Shapes and Measurements of Resonance Energies withH2+Beams

1963 ◽  
Vol 132 (4) ◽  
pp. 1710-1719 ◽  
Author(s):  
R. O. Bondelid ◽  
J. W. Butler
Keyword(s):  
Resonance Curve ◽  
Resonance Energies
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