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首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Rational synthesis of high nuclearity Mo/Fe/S clusters: The reductive coupling approach in the convenient synthesis of (Cl-4-cat)(2)Mo2Fe6S8(PR3)(6) [R = Et, Pr-n, Bu-n] and the new [(Cl-4-cat)(2)Mo2Fe2S3O(PEt3)(3)Cl]center dot 1/2(Fe(PEt3)(2)(MeCN)(
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Rational synthesis of high nuclearity Mo/Fe/S clusters: The reductive coupling approach in the convenient synthesis of (Cl-4-cat)(2)Mo2Fe6S8(PR3)(6) [R = Et, Pr-n, Bu-n] and the new [(Cl-4-cat)(2)Mo2Fe2S3O(PEt3)(3)Cl]center dot 1/2(Fe(PEt3)(2)(MeCN)(

机译:高核Mo / Fe / S团簇的合理合成:(Cl-4-cat)(2)Mo2Fe6S8(PR3)(6)的便捷合成中的还原偶联方法[R = Et,Pr-n,Bu-n ]和新的[(Cl-4-cat)(2)Mo2Fe2S3O(PEt3)(3)Cl]中心点1/2(Fe(PEt3)(2)(MeCN)(

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摘要

A general method for the synthesis of high nuclearity Mo/Fe/S clusters is presented and involves the reductive coupling of the (Et4N)(2)[(Cl-4-cat)MoOFeS2Cl2] (1) and (Et4N)(2)[Fe2S2Cl4] (H) clusters. The reaction of I and II with Fe(PR3)(2)Cl-2 or sodium salts of noncoordinating anions such as NaPF6 or NaBPh4 in the presence of PR3 (R = Et, Pr-n, or Bu-n) affords (Cl-4-cat)(2)Mo2Fe6S8(PR3)(6) [R = Et (IIIa), Pr-n (IIIb), Bu-n (IIIc)], Fe6S6(PEt3)(4)Cl-2 (IV) and (PF6)[Fe6S8((PPr3)-Pr-n)(6)] (V) as byproducts. The isolation of (Et4N)[Fe(PEt3)Cl-3] (VI), NaCl, and SPEt3 supports a reductive coupling mechanism. Cluster IV and V also have been synthesized by the reductive self-coupling of compound II. The reductive coupling reaction between I and II by PEt3 and NaPF6 in a 1:1 ratio produces the (Et4N)(2)[(Cl-4-cat)Mo(L)Fe3S4Cl3] clusters [L = MeCN (VIIa), TBF (VIIb)]. The hitherto unknown [(Cl-4-cat)(2)Mo2Fe2S3O(PEt3)(3)Cl-3] cluster (VIII) has been isolated as the 2:1 salt of the (Fe(PEt3)(2)(MeCN)(4))(2+) cation after the reductive self-coupling reaction of 1 in the presence of Fe(PEt3)(2)Cl-2. Cluster VIII crystallizes in the monoclinic space group P2(1)/c with a = 11.098(3) Angstrom, b = 22.827(6) Angstrom, c =- 25.855(6) Angstrom, beta = 91.680(4)degrees, and Z = 4. The formal oxidation states of metal atoms in VIII have been assigned as Mo-III, Mo-IV, Fe-II, and Fe-III on the basis of zero-field Mossbauer spectra. The Fe(PEt3)2(MeCN)4 cation of VIII is also synthesized independently, isolated as the BPh4- salt (IX), and has been structurally characterized. The reductive coupling of compound I also affords in low yield the new (Cl-4-cat)(2)Mo2Fe3S5(PEt3)(5) cluster (X) as a byproduct. Cluster X crystallizes in the monoclinic space group P2(1) with a = 14.811(3) Angstrom, b = 22.188(4) Angstrom, c = 21.864(4) Angstrom,beta = 100. 124(3)degrees, and Z = 4 and the structure shows very short Mo-Fe, Fe-Fe, Mo-S, Fe-S bonds. Them oxidation states of the metal atoms in this neutral cluster (X) have been assigned as (MoMoFeFeFeII)-Mo-IV-Fe-III-Fe-II-Fe-II based on zero-field Mossbauer and magnetic measurement. All Fe atoms are high spin and two of the three Fe-Fe distances are found at 2.4683(9) Angstrom and 2.4721(9) Angstrom. [References: 124]
机译:提出了一种合成高核Mo / Fe / S团簇的通用方法,该方法涉及(Et4N)(2)[(Cl-4-cat)MoOFeS2Cl2](1)和(Et4N)(2)的还原偶联。 [Fe2S2Cl4](H)团簇。 I和II在PR3(R = Et,Pr-n或Bu-n)存在下与Fe(PR3)(2)Cl-2或非配位阴离子如NaPF6或NaBPh4的钠盐反应(R = Et,Pr-n或Bu-n) -4-cat)(2)Mo2Fe6S8(PR3)(6)[R = Et(IIIa),Pr-n(IIIb),Bu-n(IIIc)],Fe6S6(PEt3)(4)Cl-2(IV )和(PF6)[Fe6S8((PPr3)-Pr-n)(6)](V)作为副产物。 (Et4N)[Fe(PEt3)Cl-3](VI),NaCl和SPEt3的分离支持还原偶联机制。簇IV和V也已经通过化合物II的还原自偶联合成。 PEt3和NaPF6以1:1的比例在I和II之间进行还原偶联反应,生成(Et4N)(2)[(Cl-4-cat)Mo(L)Fe3S4Cl3]簇[L = MeCN(VIIa),TBF (VIIb)]。迄今未知的[(Cl-4-cat)(2)Mo2Fe2S3O(PEt3)(3)Cl-3]簇(VIII)已作为(Fe(PEt3)(2)(MeCN )(4))(2+)阳离子在Fe(PEt3)(2)Cl-2存在下进行1的还原性自偶联反应后得到。簇VIII在单斜空间群P2(1)/ c中以a = 11.098(3)埃,b = 22.827(6)埃,c =-25.855(6)埃,beta = 91.680(4)度和Z结晶=4。根据零场Mossbauer光谱,已将VIII中金属原子的形式氧化态指定为Mo-III,Mo-IV,Fe-II和Fe-III。 VIII的Fe(PEt3)2(MeCN)4阳离子也可以独立合成,作为BPh4-盐(IX)分离,并已进行结构表征。化合物I的还原偶联还以低收率提供了副产物新的(Cl-4-cat)(2)Mo2Fe3S5(PEt3)(5)簇(X)。团簇X在单斜空间群P2(1)/ n中结晶,a = 14.811(3)埃,b = 22.188(4)埃,c = 21.864(4)埃,贝塔= 100. 124(3)度,以及Z = 4,并且结构显示非常短的Mo-Fe,Fe-Fe,Mo-S,Fe-S键。基于零场Mossbauer和磁测量,该中性簇(X)中金属原子的氧化态被指定为(MoMoFeFeFeII)-Mo-IV-Fe-III-Fe-II-Fe-II。所有的Fe原子都是高自旋的,并且三个Fe-Fe距离中的两个位于2.4683(9)埃和2.4721(9)埃。 [参考:124]

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