The following components were used in generating the plot: Additonal code used was developed at NIST: Other names: 2,5-Furandione; cis-Butenedioic anhydride; Dihydro-2,5-dioxofuran; Maleic acid anhydride; Toxilic anhydride; Maleic anhydride, briquettes; Anhydrid kyseliny maleinove; Maleinanhydrid; Rcra waste number U147; UN 2215; 2,5-Furanedione; M 188; NSC 137651 Permanent link for this species. Acta, 1985, A41, 937-941. Winstrom, L.O. Notice: Except where noted, spectra from this Bull. Chem. © 2018 by the U.S. Secretary of Commerce SpectraBase Spectrum ID=9PLIYs0iR12. This is my product's IR spectrum for a Diels-Alder reaction of Maleic Anhydride and Anthracene. ; Compton, R.N., ; Poling, B.E., Data from NIST Standard Reference Database 69: The National Institute of Standards and Technology (NIST) ; Offringa, J.C.A. Does my IR spectrum allow me to confirm that the structure of the product is a combination of the two reactants Maleic Anhydride and Anthracene? Thermodynamic properties of molecular organic crystals containing nitrogen, oxygen, and sulphur 1. Chem., 1973, 77, 828-831. SRD 103a – Thermo Data Engine (TDE) for pure compounds. ; Moberg, C.A.     T = temperature (K). Energy storage capacity of reversible liquid-phase Diels Alder reaction between maleic anhydride and 2-methyl furan, . of all reactions involving this species. Vapour pressures and enthalpies of sublimation, Molar heat capacities of eight compounds by adiabatic calorimetry, Data Program, but require an annual fee to access. Electron Affinities of Cyclic Unsaturated Dicarbonyls: Maleic Anhydrides, Maleimides, and Cyclopentendione, Rogers, F.E. ; McIver, R.T., Jr., Terms ; Van Miltenburg, J.C., Conn, J.B.; Kistiakowsky, G.B. [all data], Breslauer and Kabakoff, 1974 The Journal of Chemical Thermodynamics, 1983, 15, 7, 651-663, [all data], Cooper and Compton, 1973 Vapor Pressure of Pure Substances. This is my product's IR spectrum for a Diels-Alder reaction of Maleic Anhydride and Anthracene. Studies of the carbonyl group in some five-membered ring compounds by photoelectron spectroscopy, (TRC) data available from this site, much more physical Ind. Kinetics of mono-N-propylmaleate synthesis, [all data], Joshi R.M., 1970 Requires a JavaScript / HTML 5 canvas capable browser. Infrared Spectra of Reactants and Product of the Diels-Alder Reaction of Cyclopentadiene with Maleic Anhydride to form Endo-Norbornene-cis-5,6-Carboxylic Anhydride. Photoelectron spectra of 1,2-indandione, 1,3-indandione and heterocyclic analogues, DeWit, H.G.M. Data compiled by: Glushko Thermocenter, Russian Academy of Sciences, Moscow Heat of addition of cyclopentadience to maleic anhydride, J. Politeh. [all data], DeWit, DeKruif, et al., 1983 evaluated Briefly explain why. Chim., 1978, 23, 19-29. & such sites. ; De Kruif, C.G. Rev. Gheorghe Gheorghiu-Dej, Bucur., Ser. Politeh. Wilhoit, R.C. Notice: Except where noted, spectra from this collection were measured on dispersive instruments, often in carefully selected solvents, and hence may differ in detail from measurements on FTIR instruments or in other chemical environments. Stiint. errors or omissions in the Database. .971 23 921.70 899.90 754.78 714.5 634.3 543.48 531.67 416 04.68. [all data], Aldrich Chemical Company Inc., 1990 Data, 1964, 9, 595-599. Ene-grafted PP confirms the single end-grafted succinic anhydride FTIR assignment at 1792 cm−1 (CO symmetric stretching) while a disubstitution is also observed leading to a shift to a 1784 cm−1 absorption band. ; Reinhardt, P.W. [all data], Compton, Reinhardt, et al., 1974 BS - Robert L. Brown and Stephen E. Stein Ref. De Wit, H.G.M. AC - William E. Acree, Jr., James S. Chickos Ene-grafting of maleic anhydride on polypropylene previously enriched in double bonds by β-scission was promoted in order to obtain model grafted polypropylene.


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