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直接反应——一种合成镧系碘甲脒的一步法路线。

Direct Reaction - One Step Route to Synthesize Lanthanoid-iodide Formamidinates.

机构信息

School of Chemistry, Monash University, Clayton, VIC, 3800, Australia.

College of Science & Engineering, James Cook University, Townsville, QLD, 4811, Australia.

出版信息

Chem Asian J. 2023 Jul 17;18(14):e202300333. doi: 10.1002/asia.202300333. Epub 2023 May 26.

Abstract

This paper describes a novel and simple method - direct reaction of lanthanoid metals with equimolar amounts of iodine and a formamidine under ultrasonication as an effective, metal-based route to lanthanoid(III) diiodide formamidinates, namely I. N,N'-Bis(2,6-diisopropylphenyl)formamidinatodiiodidolanthanoid(III) complexes [Ln(DippForm)I (thf) ] (Ln=La, 1, Ce, 2, Tb, 3, Ho, 4, Er, 5, Tm, 6); II. N,N'-Bis(2,6-diethylphenyl)formamidinatodiiodidolanthanoid(III) complexes [Ln(EtForm)I (thf) ] (Ln=Ce, 7, Nd, 8, Gd, 9, Tb, 10, Dy, 11, Ho, 12, Er, 13, Lu, 14). III. N,N'-bis(2,6-dimethylphenyl)formamidinatodiiodidolanthanoid(III) complexes [Ln(XylForm)I (thf) ] (Ln=Ce, 15, Nd, 16, Gd, 17, Tm, 18, Lu 19); IV. N,N'-bis(phenyl)formamidinatodiiodidolanthanoid complexes [Ln(PhForm)I (thf) ] (Ln=Nd, 20, Gd, 21, Er, 22). Compound [Ce(XylForm) I(thf) ] (23) was also synthesized by the same method except the ratio of I to XylFormH was 1 : 4. Divalent N,N'-bis(2,6-diisopropylphenyl)formamidinato-iodido-lanthanoid(II) complexes [Eu(DippForm)I(thf) ] ⋅ thf (24), [Yb(DippForm)I(thf) ] ⋅ 2DippFormH (25), [Sm(DippForm)I(thf) ] ⋅ thf (26) have also been synthesized by direct reactions of the free metals, iodine and DippFormH. Interestingly, [Sm(DippForm)I (thf) ] (27) was obtained by the oxidation of [Sm(DippForm)I(thf) ] ⋅ thf (26) on exposure to air. N,N'-Bis(2,6-dimethylphenyl)formamidinatoiodidosamarium(II) [Sm(XylForm)I(thf) ] (28) was also prepared by direct reaction of Sm, iodine and XylFormH (mole ratio of I : XylFormH=1 : 2). All products have been identified by X-ray crystallography and all the trivalent complexes [Ln(Form) I ] (n=1 or 2) are stable to rearrangement.

摘要

本文描述了一种新颖而简单的方法 - 在超声条件下,等摩尔量的镧系金属与碘和甲脒直接反应,是一种有效的基于金属的合成镧系(III)二碘化甲脒的方法,得到相应的二碘化甲脒镧系(III)配合物:[Ln(DippForm)I(thf)](Ln=La,1;Ce,2;Tb,3;Ho,4;Er,5;Tm,6);[Ln(EtForm)I(thf)](Ln=Ce,7;Nd,8;Gd,9;Tb,10;Dy,11;Ho,12;Er,13;Lu,14);[Ln(XylForm)I(thf)](Ln=Ce,15;Nd,16;Gd,17;Tm,18;Lu,19);[Ln(PhForm)I(thf)](Ln=Nd,20;Gd,21;Er,22)。化合物[Ce(XylForm)I(thf)](23)也是通过相同的方法合成的,只是碘与 XylFormH 的摩尔比为 1:4。二价 N,N'-双(2,6-二异丙基苯基)甲脒碘化物-二价镧系金属配合物[Eu(DippForm)I(thf)]·thf(24),[Yb(DippForm)I(thf)]·2DippFormH(25),[Sm(DippForm)I(thf)]·thf(26)也是通过自由金属、碘和 DippFormH 的直接反应合成的。有趣的是,[Sm(DippForm)I(thf)](27)是通过暴露于空气中氧化[Sm(DippForm)I(thf)]·thf(26)得到的。N,N'-双(2,6-二甲基苯基)甲脒碘代钐(II)[Sm(XylForm)I(thf)](28)也是通过 Sm、碘和 XylFormH(I:XylFormH 的摩尔比为 1:2)的直接反应制备的。所有产物均通过 X 射线晶体学进行了鉴定,所有三价配合物[Ln(Form)I](n=1 或 2)都稳定,不会发生重排。

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