Potentiometric and spectrophotometric studies of complexes of hydrolysis products of amylose with iodine and potassium iodide.
نویسنده
چکیده
Grassmann, W. & Hannig, K. (1950). Z. angew. Chem. 62, 170. Greenway, R. M., Kent, P. W. & Whitehouse, M. W. (1953). Research, Lond., 6, 6S. Hach, R. J. & Rundle, R. E. (1951). J. Amer. chem. Soc. 73, 4321. Hanes, C. S. (1937). New Phytol. 36, 189. Higginbotham, R. S. (1949). Shirley Int. Mem. 23, 159, 171. Hopkins, R. H., Stopher, E. G. & Dolby, D. E. (1940). J. Inst. Brew. 46, 426. Isherwood, F. A. (1949). Proc. 18t Int. Congr. Biochem. Cambridge. Abstract no. 339/11, p. 515. Jaenicke, L. (1952). Naturwissen8chaften, 39, 86. James, A. T. & Synge, R. L. M. (1951). Biochem. J. 50, 109. Jeanes, A., Wise, C. F. & Dimler, R. J. (1951). Analyt. Chem. 23, 415. Meyer, K. H. & Gonon, W. F. (1951). Helv. chim. acta, 34, 294. Micheel, F. & Kamp, F. P. van de (1952). Angew. Chem. 64, 607. Michl, H. (1952). Mh. Chem. 83, 737. Mooney, R. C. L. (1935). Z. Kristallogr. 90, 143. Mould, D. L. (1954). Biochem. J. 58, 593. Mould, D. L. & Synge, R. L. M. (1954). Biochem. J. 58, 571. Norberg, E. & French, D. (1950). J. Amer. chem. Soc. 72, 1202. Posternak, T. (1935). Helv. Chim. acta. 18, 1351. Posternak, T. (1951). J. biol. Chem. 188, 317. Rundle, R. E. & Baldwin, R. R. (1943). J. Amer. chem. Soc. 65, 554. Samec, M. & Blinc, M. (1938). Kolloidbeihefte. 47, 371. Saric, S. P. & Schofield, R. K. (1946). Proc. Roy. Soc. A, 185, 431. Saverborn, S. (1945). Acidpolyuronides. Uppsala: Almqvist & Wiksells Boktryckeri AB. Through Chem. Ab8tr. (1947), 41, 396c. Schoch, T. J. (1942). J. Amer. chem. Soc. 64, 2957. Speiser, R., Copley, M. J. & Nutting, G. C. (1947). J. phy8. Chem. 51, 117. Stein, R. S. & Rundle, R. E. (1948). J. chem. Phy8. 16, 195. Svensson, H. (1948). Advanc. Protein Chem. 4, 251. Svensson, H. & Brattsten, I. (1949). Ark. Kemi, 1, 401. Swanson, M. A. (1948). J. biol. Chem. 172, 825. Synge, R. L. M. (1951). Biochem. J. 49, 642. Theorell, H. & Akeson, A. (1942). Ark. Kemi Min. Geol. 16A, no. 8. Whelan, W. J. & Bailey, J. M. (1954). Biochem. J. 58, 560. Wolfrom, M. L. & Rice, F. A. H. (1947). J. Amer. chem. Soc. 69, 2918. Woodin, A. M. (1952). Biochem. J. 51, 319.
منابع مشابه
Spectrophotometric Study of the Complexation of Iodine and Bromine with Tetrabutylammonium Halides and Cryptand 222 in Dichloromethane Solution
A spectrophotometric study concerning the interactoin between iodine and bromine with tetrabutylammonium iodide (TBAI), tetrabutyl- ammonium bromide (TBABr) and cryptand 222 (C222) has been performed in dichloromethane solution at 25°C. The results are indicative of the formation of TBA+X3- and C222X+X3- t...
متن کاملSpectroscopic Study of Charge Transfer Complexes of Dibenzo-24-crown-8 (DB24C8) with Iodine in Three Chlorinated Solvents
Charge Transfer (CT) complexes formed between dibenzo-24-crown-8 (DB24C8) as an electron donor with the σ-electron acceptor iodine (I2) in chloroform, dichloromethane, and 1,2-dichloroethane solutions have been studied by different spectroscopic techniques at room temperature. The spectral studies of the complexes were det...
متن کاملAntioxidant and immune gene expression in zebra fish (Danio rerio)
Iodine is the main ingredient produced by the thyroid hormone, which playa a central role in the metabolism and the immune system. The present study aims to evaluate the effects of feeding Artemia fransiscana enriched with potassium iodide on antioxidant and immune gene expression in zebra fish (Danio rerio). Zebra larvae with an average weight of 2±0.01 mg were randomly distributed into 4 trea...
متن کاملThe complex of amylose and iodine
The organization of polyiodide chains in the amylose-iodine complex was investigated by Raman spectroscopy, by UV/vis, and by second-derivative UV/vis spectroscopies complemented by semiempirical calculations based on a simple structural model. The Raman spectra indicate that the primary substructures of the polyiodide chains are I–3; and I; sub-units. The second derivatives of the UV/vis spect...
متن کاملTitrimetric and spectrophotometric assay of diethylcarbamazine citrate in formulations using iodate and iodide mixture as reagents
One titrimetric and two spectrophotometric methods are proposed for the determination of diethylcarbamazine citrate (DEC) in bulk drug and in formulations using potassium iodate and potassium iodide as reagent. The methods employ the well-known analytical reaction between iodate and iodide in the presence of acid. In titrimetry (method A), the drug was treated with a measured excess of thiosulf...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- The Biochemical journal
دوره 58 4 شماره
صفحات -
تاریخ انتشار 1954