Physicochemical characterization of novel Schiff bases derived from developed bacterial cellulose 2,3-dialdehyde

被引:54
作者
Keshk, Sherif M. A. S. [1 ,2 ]
Ramadan, Ahmed M. [1 ,3 ]
Bondock, Samir [1 ,4 ]
机构
[1] King Khalid Univ, Fac Sci, Dept Chem, POB 9004, Abha 61413, Saudi Arabia
[2] Ain Shams Univ, Inst Environm Studies & Res, Dept Basic Sci, Cairo 11566, Egypt
[3] Univ Alexandria, Fac Sci, Dept Chem, Alexandria, Egypt
[4] Mansoura Univ, Fac Sci, Dept Chem, Mansoura, Egypt
关键词
Bacterial cellulose; Periodate oxidation; Aldehyde content; Schiff bases; X-ray diffractogram; NASCENT MICROBIAL CELLULOSE; FLUORESCENT BRIGHTENER; CRYSTAL-STRUCTURE; TRANSITIONS;
D O I
10.1016/j.carbpol.2015.03.038
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
The synthesis of two novel Schiff's bases (cellulose-2,3-bis-[(4-methylene-amino)-benzene-sulfonamide] (5) & cellulose-2,3-bis-[(4-methylene-amino)-N-(thiazol-2-yl)-benzenesulfonamide] (6) via condensation reactions of periodate oxidized developed bacterial cellulose ODBC (2) with sulfa drugs [sulfanilamide (3) & sulfathiazole (4)1 was reported. The physicochemical characterization of the condensation products was performed using FTIR, H-1 NMR,C-13 NMR spectral analyses, X-ray diffraction and DTA. The ODBC exhibited the highest degree of oxidation based on the aldehyde group number percentage (82.9%), which confirms the highest reactivity of developed bacterial cellulose [DBC (1)]. The X-ray diffractograms indicated an increase in the interplanar distance of the cellulose Schiff base (6) compared to ODBC (2) due to sulfathiazole (4) inclusion between ODBC (2) sheets corresponding to the (1 (1) over bar 0) plane. In addition, the aldehyde content of Schiff base (6) was (20.8%) much lower than that of Schiff base (5) (41.5%). These results confirmed the high affinity of sulfathiazole (4) to the ODBC (2) chain, and the substantial changes in the original properties of ODBC were due to these chemical modifications rather than the sulfanilamide (3). (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:246 / 251
页数:6
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