Alanazi Abdulaziz M, McNaughter Paul D, Alam Firoz, Vitorica-Yrezabal Inigo J, Whitehead George F S, Tuna Floriana, O'Brien Paul, Collison David, Lewis David J
Department of Chemistry, University of Manchester, Oxford Road, Manchester M13 9PL, U.K.
Department of Materials, University of Manchester, Oxford Road, Manchester M13 9PL, U.K.
ACS Omega. 2021 Oct 11;6(42):27716-27725. doi: 10.1021/acsomega.1c02907. eCollection 2021 Oct 26.
Manganese(II) xanthate complexes of the form [Mn(SCOR)(TMEDA)], where TMEDA = tetramethylethylenediamine and R = methyl (), ethyl (), -propyl (), -butyl (), -pentyl (), -hexyl (), and -octyl (), have been synthesized and structures elucidated using single-crystal X-ray diffraction. Complexes - were used as molecular precursors to synthesize manganese sulfide (MnS). Olelyamine-capped nanocrystals have been produced hot injection, while the doctor blading followed by thermolysis yielded thick films. Free-standing polycrystalline powders of MnS are produced by direct thermolysis of precursor powders. All thermolysis techniques produced cubic MnS, as confirmed by powder X-ray diffraction, scanning electron microscopy, energy-dispersive X-ray spectroscopy, and Raman spectroscopy. Magnetic measurements reveal that the α-MnS nanocrystals exhibit ferromagnetic behavior with a large coercive field strength ( 0.723 kOe for 6.8 nm nanocrystals).
已合成了通式为[Mn(SCOR)(TMEDA)]的二硫代黄原酸锰(II)配合物,其中TMEDA = 四甲基乙二胺,R = 甲基()、乙基()、丙基()、丁基()、戊基()、己基()和辛基(),并通过单晶X射线衍射对其结构进行了阐释。配合物 - 被用作合成硫化锰(MnS)的分子前驱体。通过热注射制备了油胺包覆的纳米晶体,而刮刀法随后进行热解得到了厚膜。通过前驱体粉末的直接热解制备了MnS的自立多晶粉末。粉末X射线衍射、扫描电子显微镜、能量色散X射线光谱和拉曼光谱证实,所有热解技术均生成了立方MnS。磁性测量表明,α-MnS纳米晶体表现出铁磁行为,具有较大的矫顽场强(6.8 nm纳米晶体为0.723 kOe)。