首页> 外文期刊>Organometallics >Synthesis and redox properties of (3-phenothiazinomesityl)- and (4-phenothiazinoduryl)dimesitylphosphines and the corresponding arsines
【24h】

Synthesis and redox properties of (3-phenothiazinomesityl)- and (4-phenothiazinoduryl)dimesitylphosphines and the corresponding arsines

机译:(3-吩噻嗪并二甲双胍)-和(4-吩噻嗪并二氢呋喃基)二甲烯丙基膦和相应的a烷的合成及氧化还原性质

获取原文
获取原文并翻译 | 示例
           

摘要

To construct the novel redox systems possessing the trimesitylphosphine- or trimesitylarsine-type substructure as a reversible redox site, dimesity](3-phenothiazinomesityl)phosphine, dimesityl(4-phenothiazinoduryl)phosphine, and the corresponding arsines were synthesized (mesityl = 2,4,6-trimethylphenyl, duryl = 2,3,5,6-tetramethylphenyl). The key synthetic intermediates, (3-bromomesityl)-dimesitylphosphine, (4-bromoduryl)dimesitylphosphine, and the analogous arsines were prepared by successive addition of the corresponding Grignard reagents to phosphorus or arsenic trichloride. The (bromoaryl)phosphines and -arsines were converted to the corresponding (iodoaryl)phosphines and -arsines and coupled with phenothiazine in the presence of copper to afford the phenothiazinophosphino- and phenothiazinoarsinobenzenes. The cyclic voltammograms of the phenothiazinopnictogenobenzenes thus obtained exhibit two-step redox waves corresponding to oxidation on the pnictogen as well as phenothiazine redox centers. The phenothiazino group contributes to stability of the redox systems, and the phenothiazinophosphinobenzenes display two-step nearly reversible redox waves at -78 degrees C. On the other hand, the cyclic voltammograms of the phenothiazinoarsinobenzenes consist of the first reversible wave followed by the second irreversible wave, suggesting decomposition at the unstable arsenic redox center. The pnictogen redox centers of the phenothiazinopnictogenobenzenes are unstable as compared with those of the corresponding trimesityl derivatives. Chemical oxidation of the phenothiazinophosphinobenzenes and phenothiazinoarsinobenzenes by tris(4-bromophenyl)aminium perchlorate, which can oxidize trimesitylphosphine and trimesitylarsine to the corresponding cation radicals, was studied by EPR. However, only the nitrogen-centered cation radical was observed probably because of the instability of the phosphorus as well as arsenic radical centers.
机译:为了构建具有三苯甲基膦或三苯甲基赖氨酸型亚结构作为可逆氧化还原位点的新型氧化还原系统,合成了二元](3-吩噻嗪金属甲酰基)膦,二苯甲基(4-苯并噻嗪二氢基)膦和相应的砷化氢(甲磺酰基= 2,4 (6-6-三甲基苯基,duryl = 2,3,5,6-四甲基苯基)。通过将相应的格氏试剂连续添加到磷或三氯化砷中,可以制备关键的合成中间体(3-溴甲磺酰基)-二甲磺酰基膦,(4-溴二甲酰基)二甲磺酰基膦和类似的a类化合物。将(溴代芳基)膦和-s氨酸转化为相应的(碘代芳基)膦和-ar氨酸,并在铜存在下与吩噻嗪偶联,得到吩噻嗪基膦基-和吩噻嗪基砷基苯。如此获得的吩噻嗪并氮杂苯的循环伏安图显示出两步氧化还原波,对应于在该光电子原上的氧化以及吩噻嗪氧化还原中心。吩噻嗪基基团有助于氧化还原系统的稳定性,酚噻嗪膦基苯在-78摄氏度下显示两步几乎可逆的氧化还原波。另一方面,吩噻嗪基砷化苯的循环伏安图包括第一个可逆波,然后是第二个不可逆波。波动,表明在不稳定的砷氧化还原中心分解。与相应的三苯甲基叔胺衍生物相比,吩噻嗪并氮杂苯的光致氧化还原中心不稳定。通过EPR研究了三(4-溴苯基)高氯酸铵化学氧化苯并噻嗪膦基苯和苯并噻嗪砷基苯,其可将三苯甲基膦和三苯甲基赖氨酸氧化成相应的阳离子自由基。然而,可能仅观察到以氮为中心的阳离子自由基,这可能是由于磷以及砷自由基中心的不稳定性。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号