1980
DOI: 10.1016/s0020-1693(00)80081-x
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Labile 1,10-phenanthroline N-oxide complexes with tin(II) and (IV) halides

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Cited by 4 publications
(4 citation statements)
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“…In alternative, the same synthesis also works in isopropanol. The yield was 92%, and the product was characterized by elemental analysis assuming that the final formula of the compound is Sn(phen)Cl 2 as reported by Owens et al 49 The found elemental analysis percentages seemed to confirm that assumption (C calc , 38.96%; N calc , 7.58%; H calc , 2.16%; C found , 36.83%; N found , 6.82%; H found , 2.09%). The suggested structure is shown in Figure 1a.…”
Section: Synthesis Of Sn(phen)cl 2 (Sn-phen) Complexsupporting
confidence: 64%
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“…In alternative, the same synthesis also works in isopropanol. The yield was 92%, and the product was characterized by elemental analysis assuming that the final formula of the compound is Sn(phen)Cl 2 as reported by Owens et al 49 The found elemental analysis percentages seemed to confirm that assumption (C calc , 38.96%; N calc , 7.58%; H calc , 2.16%; C found , 36.83%; N found , 6.82%; H found , 2.09%). The suggested structure is shown in Figure 1a.…”
Section: Synthesis Of Sn(phen)cl 2 (Sn-phen) Complexsupporting
confidence: 64%
“…Therefore, SnCl 2 ·2H 2 O and 1,10-phenantroline (1:2 molar ratio in EtOH solution) were mixed. A yellow precipitate was immediately formed; the solution was filtered within 5–10 min to avoid the decomposition product to form as observed by Owens, which adopted N oxide-phenanthroline as a ligand . The product was finally washed with ice-cold ethanol and then dried overnight at 40 °C.…”
Section: Methodsmentioning
confidence: 99%
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“…Within this family of compounds, only limited information is available on 1,10-phenanthroline-1-Noxide (phenO) and its derivatives. A few metal complexes of phenO have been synthesized in solid phase since the 1970s, but the detailed characterization of these compounds is not available [18][19][20][21][22][23][24][25][26][27][28]. Recent results show that platinum(II) complexes of phenO have broad potential as oxygen atom transfer reagents because of their ability to activate the N-O bond [29].…”
Section: Introductionmentioning
confidence: 99%