Klepka Marcin T, Nedelko Nataliya, Greneche Jean-Marc, Lawniczak-Jablonska Krystyna, Demchenko Iraida N, Slawska-Waniewska Anna, Rodrigues Clovis A, Debrassi Aline, Bordini Cristiani
Institute of Physics, Polish Academy of Sciences, Al. Lotnikow 32/46 PL-02668, Warsaw, Poland.
Biomacromolecules. 2008 Jun;9(6):1586-94. doi: 10.1021/bm800044y. Epub 2008 May 8.
The iron crosslinked chitosan (Ch-Fe-CL) and N-carboxylmethyl chitosan (N-CM-Ch-Fe) complexes were studied by complementary techniques: structurally sensitive Mössbauer and X-ray absorption methods, as well as static magnetic measurements. A detailed and consistent description of these complexes including, besides the overall magnetic behavior, the spin ordering and local atomic structure around Fe ions is presented. Fe atoms in the investigated samples are mostly penta-coordinated and appear in a high spin Fe (3+) ionic state. In Ch-Fe-CL, two kinds of Fe near neighbors are equally probable and several Fe atoms are situated in the second coordination sphere. The magnetic interactions between these Fe ions lead to a sperimagnetic-like ordering. In N-CM-Ch-Fe, only one Fe neighborhood was found. Other Fe atoms were identified neither in the first nor in the second coordination sphere, but the third coordination sphere indicates the presence of Fe atoms. The magnetic coupling between these atoms is antiferromagnetic, but the dominant part of Fe in this sample remains in a paramagnetic state.
通过互补技术对铁交联壳聚糖(Ch-Fe-CL)和N-羧甲基壳聚糖(N-CM-Ch-Fe)配合物进行了研究:结构敏感的穆斯堡尔和X射线吸收方法以及静态磁测量。除了整体磁行为外,还给出了这些配合物的详细且一致的描述,包括铁离子周围的自旋排序和局部原子结构。所研究样品中的铁原子大多为五配位,呈高自旋Fe(3+)离子态。在Ch-Fe-CL中,两种铁近邻的可能性相同,且有几个铁原子位于第二配位球中。这些铁离子之间的磁相互作用导致类似亚铁磁性的排序。在N-CM-Ch-Fe中,仅发现一种铁邻域。在第一和第二配位球中均未发现其他铁原子,但第三配位球表明存在铁原子。这些原子之间的磁耦合是反铁磁性的,但该样品中铁的主要部分仍处于顺磁状态。