2019
DOI: 10.1007/s10904-019-01264-3
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The Effects of Temperature on Iron Sulfide Nanocrystals Prepared from Thermal Decomposition of Bis-(N-methylbenzyldithiocarbamato)iron(II) Complex

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Cited by 8 publications
(5 citation statements)
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“…Thus, while heating [Fe­(S 2 CNR 2 ) 2 ], [Fe­(S 2 CNR 2 ) 3 ] and cis -[Fe­(CO) 2 (S 2 CNR 2 ) 2 ] in OLA all lead to the generation of the same decomposition species, postulated as [Fe­(S 2 CNR 2 ) 2 (OLA) n ], the nature of the final products still depends (to some extent) on the SSP used. Two further publications claim to use [Fe­(S 2 CNR 2 ) 2 ] for solvothermal decomposition, , but most likely they are the corresponding Fe­(III) complexes as reactions were not carried out under an inert atmosphere.…”
Section: Binary Sulfidesmentioning
confidence: 99%
“…Thus, while heating [Fe­(S 2 CNR 2 ) 2 ], [Fe­(S 2 CNR 2 ) 3 ] and cis -[Fe­(CO) 2 (S 2 CNR 2 ) 2 ] in OLA all lead to the generation of the same decomposition species, postulated as [Fe­(S 2 CNR 2 ) 2 (OLA) n ], the nature of the final products still depends (to some extent) on the SSP used. Two further publications claim to use [Fe­(S 2 CNR 2 ) 2 ] for solvothermal decomposition, , but most likely they are the corresponding Fe­(III) complexes as reactions were not carried out under an inert atmosphere.…”
Section: Binary Sulfidesmentioning
confidence: 99%
“…Figure exhibits the UV–vis absorbance spectra of as-synthesized PDTC, Cu­[PDTC] 2 , and Co­[PDTC] 2 complexes. Here, peaks at 253 nm were attributed to π → π* transitions related to the N–CS group where the absorption band at 286 nm was associated with transitions of the S–CS group present in PDTC (Figure a) . The UV–vis spectra of Cu­[PDTC] 2 show an additional peak at 432 nm which is due to the electronic transition from CS π* orbitals to 3d orbitals of Cu­(II) (Figure c), whereas the electronic transition from CS π* orbitals to the 3d orbital of Co­(II) leads to an absorption band at 394 nm for the Co­[PDTC] 2 complex (Figure b).…”
Section: Resultsmentioning
confidence: 97%
“…[54] Peaks appeared at 1497, 1438, 1394, and 1289 cm À 1 due to stretching vibration of CÀ N bond of À CÀ NÀ C and À CÀ N À S units. [55,56] Moreover, peaks in the region of 1300-900 cm À 1 were associated with the stretching vibration of C=S and CÀ S bonds of À CSS À group. [56][57][58] Weak peak at 758 cm À 1 can be assigned to À CH 2 rocking mode.…”
Section: Resultsmentioning
confidence: 98%
“…ATR‐FTIR spectrum of DEDTC showed peaks at 2952 and 2850 cm −1 are corresponding to asymmetric and symmetric stretching of −CH 3 group present in DEDTC, respectively (Figure 1b–i) [54] . Peaks appeared at 1497, 1438, 1394, and 1289 cm −1 due to stretching vibration of C−N bond of −C - ${-}$ N - ${-}$ C and −C - ${-}$ N - ${-}$ S units [55,56] . Moreover, peaks in the region of 1300–900 cm −1 were associated with the stretching vibration of C=S and C−S bonds of -CSS- ${-{CSS}^{-}}$ group [56–58] .…”
Section: Resultsmentioning
confidence: 98%