Preparation of chromium(III) complexes with a series of tetraazacycloalkanes, [12]aneN4 to [16]aneN4, and solid-state thermal isomerisation of cis-[CrCl2([15]- or [16]aneN4)]+
作者:Eiji Itoh、Kenji Yamamoto、Mitsuo Funato、Masatatsu Suzuki、Akira Uehara
DOI:10.1016/0040-6031(92)80048-2
日期:1992.1
[16]aneN 4 )] + with sulphinyl chloride in methanol. [Cr(C 2 O 4 )(mac)] + complexes were prepared by the reaction of the respective dihalogeno complexes with NaHC 2 O 4 . Relative ligand field strengths of macs were estimated from D q xy values for trans-dihalogeno complexes, and D q av values for cis-dihalogeno and oxalato complexes as follows: cyclam > isocyclam > [15]aneN 4 > [16]aneN 4 for the trans
摘要 制备了一系列顺式和/或反式-[CrX 2 (mac)] + 和[Cr(C 2 O 4 )(mac) + 形式的铬(III)配合物,其中X为F - , Cl - 或 B - 离子,并且 mac 是 1,4,7,10-四氮杂环十二烷 ([12]aneN 4 ), 1,4,7,10-四氮杂环十三烷 ([13]aneN 4 ), 1,4,8, 11-四氮杂环十四烷 ([14]aneN 4 , cyclam), 1,4,7,11-四氮杂环十四烷 ([14]aneN4, isocyclam), 1,4,8,12-四氮杂环十五烷 ([15]aneN4), 或 1, 5,9,13-四氮杂环十六烷([16]aneN 4 )。当反式-[CrF 2 (py) 4 ] + 和[CrCl 3 (thf) 3 ]用作制备[CrX 2 (mac)] + 配合物的起始材料时,[12]仅形成顺式异构体- 和[13]aneN