Measurement and development of solubility correlations for tritolylamine in twelve organic solvents

Industrial and Engineering Chemistry Research

Volumn 44, Issue 4, 2005, Pages 970-976

  Manifar, Touraj ^a   Rohani, Sohrab ^a   Saban, Marko ^b  

^a UNIVERSITY OF WESTERN ONTARIO   (Canada)

^b XEROX RESEARCH CENTRE OF CANADA   (Canada)

Author keywords

[No Author keywords available]

Indexed keywords

DIFFERENTIAL SCANNING CALORIMETRY; GRAVIMETRIC ANALYSIS; MOLECULAR ORIENTATION; SOLUBILITY; SOLVENTS; SPECIFIC HEAT;

ENANTIOMERS; HEAT OF FUSION; POLARITY INDEX; POLYMORPHS;

AMINES;

2 BUTANONE; 2 PROPANOL; ALCOHOL; AMINE; BENZENE; DECANE; HEPTANE; HEXADECANE; HEXANE; METHANOL; OCTANE; ORGANIC SOLVENT; PROPANOL; TOLUENE;

SOLVENT;

ARTICLE; CHEMICAL STRUCTURE; CONCENTRATION (PARAMETERS); CORRELATION ANALYSIS; DENSITY; DIFFERENTIAL SCANNING CALORIMETRY; GRAVIMETRY; PREDICTION; SOLUBILITY; TEMPERATURE DEPENDENCE;

EID: 13544255388     PISSN: 08885885     EISSN: None     Source Type: Journal    
DOI: 10.1021/ie049352v     Document Type: Article

References (41)

1. Singer, R. A.; Sadighi, J. P.; Buchwald, S. L. A General Synthesis of End Functionalized Oligoanilines via Paladium-Catalyzed Amination. J. Am. Chem. Soc. 1998, 120, 213-214.
2. Hong, Y.; Senanayake, C. H.; Xiang, T.; Vandenbossche, C. P.; Tanoury, G. J.; Bakale, R. P.; Wald, S. A. Remarkably Selective Palladium-Catalyzed Amination Process: Rapid Assembly of Multiamino Based Structure. Tetrahedron Lett. 1998, 39, 3121-3124.
3. Negwer, M. Organic Drugs and Their Synonyms; Akademie Verlag GmbH: Berlin, 1994.
4. Louie, J.; Hartwig, J. F. Discrete High Molecular Weight Triarylamine Dendrimers Prepared by Palladium Catalyzed Amination. J. Am. Chem. Soc. 1997, 119, 11695-11696.
5. Brantly, T. B.; Contois, L. E.; Fox, C. J. Photoconductive Elements Containing Substituted Triarylamine Photoconductors. U.S. Patent 3,567,450, 1971.
6. Brantly, T. B.; Contois, L. E.; Fox, C. J. Photoconductive Elements Containing as Photoconductors Triarylamines Substituted by Active Hydrogen Containg Groups. U.S. Patent 3,658,520, 1972.
7. Klupfel, K.-W.; Sus, O.; Behmenburg, H.; Neugebauer, W. Material for Electrophotographic Purposes. U.S. Patent 3,180,730, 1965.
8. D'lorio, M. Molecular Materials for Microelectronics. Can. J. Phys. 2000, 78, 231-241.
9. Kaliowski, J. Electroluminescence in Organics. J. Phys. D: Appl. Phys. 1999, 32, R-179-R-250.
10. Mitschke, U.; Bäuerle, P. The Electroluminescence of Organic Materials. J. Mater. Chem. 2000, 10, 1471-1507.
11. Borsenberger, P. M.; Wiess, D. S. Organic Photoreceptors for Xerography; Marcel Dekker Inc.: New York, 1998.
12. Law, K.-Y. Organic Photoconductive Materials: Recent Trends and Developments. Chem. Rev. 1993, 93, 449-486.
13. Loutfy, R. O.; Hor, A. M.; Hsiao, C. K.; Baranyi, G.; Kazmaier, P. Organic Photoconductive Materials. Pure Appl. Chem. 1988, 60, 1047-1054.
14. Dodabalapur, A.; Jordan, R.; Strakelj, M. Blue Emitting Materials and Electroluminescent Devices Containing These Materials. U.S. Patent 5,904,994, 1999.
15. Forest, S. R.; Burrows, P.; Garbuzov, D. Z. Light Emitting Devices Having High Brightness. U.S. Patent 6,125,226, 2000.
16. Hosokawa, C. Highly Efficient Blue Electroluminescence from a Distyrylarylene Emitting Layer With a New Dopant. Appl. Phys. Lett. 1995, 67, 3853-3855.
17. Prausnitz, J. M.; Lichtenthaler, R. N.; Azevedo, E. G. Molecular Thermodynamics of Fluid-Phase Equilibria, 3rd ed.; Prentice Hall International: Upper Saddle River, NJ, 1999; pp 638-670.
18. Scatchard, G.; Wilson, G. M.; Satkiewicz, F. G. Vapor-Liquid Equilibrium. X. An Apparatus for Static Equilibrium Measurements. J. Am. Chem. Soc. 1964, 86, 125-127.
19. Wilson, G. M. Vapor-Liquid Equilibrium. XI. A New expression for the Excess Free Energy of Mixing. J. Am. Chem. Soc. 1964, 86, 127-130.
20. Abrams, D. S.; Prausnitz, J. M. Statistical Thermodynamics of Liquid Mixture. A New Expression for the Excess Gibbs Energy of Partly and Completely Miscible Systems. AIChE J. 1975, 21, 116-128.
21. Fredenslund, A.; Jones, R. L.; Prausnitz, J. M. Group Contribution Estimation of Activity Coefficients in Nonideal Liquid Mixtures. AIChE J. 1975, 21, 1086-1099.
22. Derr, E. L.; Deal, C. H. Predicted Compositions during Mixed Solvent Evaporation from Resin Solutions Using the Analytical Solution of Groups Methodo. Adv. Chem. Ser. 1973, 124.
23. Yaws, C. L.; Wang, M. A.; Satyro, M. A. Chemical Properties Hand Book: Physical, Thermodynamic, Environmental, Transport, Safety, and Health Related Properties for Organic and Inorganic Chemicals; McGraw-Hill: New York, 1999; pp 340-363.
24. Goodbrand, H. B.; Nan-Xing, H. Ligand Accelerated Catalysis of the Ullmann Condensation: Application to Hole Conducting Triarylamines. J. Org. Chem. 1999, 64, 670-674.
25. Manifar, T.; Bender, T.; Goodbrand, H. B.; Gaynor, R.; Saban, M.; Rohani, S. Observations Regarding the Copper(I) Mediated Ligand Accelerated Ullmann-type Coupling of Anilines with Aryliodides: Ligand Selection and Determination of Reaction Kinetics. Ind. Eng. Chem. Res., manuscript accepted.
26. Helt, J. E.; Larson, M. A. Effect of Temperature on the Crystallization of Potassium Nitrate by Direct Measurement of Supersaturation. AIChE J. 1977, 23, 822-830.
27. Sikdar, S. K.; Randolph, A. D: Secondary Nucleation of two Fast Growth System in a Mixed Suspension Crystallizer: Magnesium Sulfate and Citric Acid Water System. AIChE J. 1976, 22, 110-117.
28. Mersmann, A.; Kind, M. Modeling of Chemical Process Equipment: Modeling and Design of Crystallizers. Int. Chem. Eng. 1989, 29, 616-626.
29. Mullin, J. W. Crystallization, 1st ed.; Butterworth-Heinmann Ltd.: Oxford, U.K., 1993.
30. Rohani, S. Crystallization Kinetics, Modeling and Control. Chem. Eng. 1998, 5, 173-193.
31. Tadayyon, A.; Rohani, S.; Bennett, M. Estimation of Nucleation and Growth Kinetics of Ammonium Sulphate from Transients of a Cooling Batch Seeded Crystallizer. Ind. Eng. Chem. Res. 2002, 41, 6181-6193.
32. Raphael, M.; Rohani, S. On-Line Estimation of Solids Concentrations and Mean Particle Size Using a Turbidimetry Method. Powder Technol. 1996, 89, 157-163.
33. Thatipamala, R.; Rohani, S.; Hill, G. A. Spectrophotometric Method For High Biomass Concentration Measurements. Biotechnol. Bioeng. 1991, 38, 1007-1011.
34. Thatipamala, R.; Rohani, S.; Hill, G. Online Monitoring of a Wide Range of Biomass Concentrations Based on a New Equation Using a Spectrophotometer- Process-Control Applications. J. Biotechnol. 1994, 38, 33-42.
35. Berstein, J. Polymorphism in Molecular Crystals; Oxford University Press: New York, 2002.
36. Brittain, H. G. Polymorphism in Pharmacetical Solids; Marcel Dekker: New York, 1999; p 300.
37. Hanai, T. HPLC, A Practical Guide; Royal Society of Chemistry: Cambridge, U.K., 1999.
38. Goodbrand, H. B. Arylamine Processes. U.S. Patent 5,648,542, 1997.
39. Goodbrand, H. B. Triarylamine Processes. U.S. Patent 5,654,482, 1997.
40. Goodbrand, H. B.; Hu, N.-X.; Ong, B. S. Arylamine Processes. U.S. Patent 5,705,697, 1998.
41. Anderson, T. F.; Prausnitz, J. M. Application of the UNIQUAC equation to calculation of multicomponent phase equilibriums. 2. Liquid-liquid equilibriums. Ind. Eng. Chem. Process Des. Dev. 1978, 17, 561-567.