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The molecular Pt nanocluster [Pt27(CO)31]4- (14-) was obtained by thermal decomposition of [Pt15(CO)30]2- in tetrahydrofuran under a H2 atmosphere. The reaction of 14- with increasing amounts of HBF4·Et2O afforded the previously reported [Pt26(CO)32]2- (32-) and [Pt26(CO)32]- (3-). The new nanocluster 14- was characterized by IR and UV-visible spectroscopy, single-crystal X-ray diffraction, direct-current superconducting quantum interference device magnetometry, cyclic voltammetry, IR spectroelectrochemistry (IR SEC), and electrochemical impedance spectroscopy. The cluster displays a cubic-close-packed Pt27 framework generated by the overlapping of four ABCA layers, composed of 3, 7, 11, and 6 atoms, respectively, that encapsulates a fully interstitial Pt4 tetrahedron. One Pt atom is missing within layer 3, and this defect (vacancy) generates local deformations within layers 2 and 3. These local deformations tend to repair the defect (missing atom) and increase the number of Pt-Pt bonding contacts, minimizing the total energy. The cluster 14- is perfectly diamagnetic and displays a rich electrochemical behavior. Indeed, six different oxidation states have been characterized by IR SEC, unraveling the series of 1n- (n = 3-8) isostructural nanoclusters. Computational studies have been carried out to further support the interpretation of the experimental data.

The molecular nanocluster [Ni36–xPd5+x(CO)46]6– (x = 0.41) (16–) was obtained from the reaction of [NMe3(CH2Ph)]2[Ni6(CO)12] with 0.8 molar equivalent of [Pd(CH3CN)4][BF4]2 in tetrahydrofuran (thf). In contrast, [Ni37–xPd7+x(CO)48]6– (x = 0.69) (26–) and [HNi37–xPd7+x(CO)48]5– (x = 0.53) (35–) were obtained from the reactions of [NBu4]2[Ni6(CO)12] with 0.9–1.0 molar equivalent of [Pd(CH3CN)4][BF4]2 in thf. After workup, 35– was extracted in acetone, whereas 26– was soluble in CH3CN. The total structures of 16–, 26–, and 35– were determined with atomic precision by single-crystal X-ray diffraction. Their metal cores adopted cubic close packed structures and displayed both substitutional and compositional disorder, in light of the fact that some positions could be occupied by either Ni or Pd. The redox behavior of these new Ni–Pd molecular alloy nanoclusters was investigated by cyclic voltammetry and in situ infrared spectroelectrochemistry. All three compounds 16–, 26–, and 35– displayed several reversible redox processes and behaved as electron sinks and molecular nanocapacitors. Moreover, to gain insight into the factors that affect the current–potential profiles, cyclic voltammograms were recorded at both Pt and glassy carbon working electrodes and electrochemical impedance spectroscopy experiments performed for the first time on molecular carbonyl nanoclusters., The synthesis, molecular structure, electrochemical, and infrared spectroelectrochemical behavior of three new atomically precise Ni−Pd alloy carbonyl nanoclusters are reported, together with the first electrochemical impedance spectroscopy investigation of redox active carbonyl nanoclusters.

This article describes a rare case of cluster core isomerism in a large molecular organometallic nanocluster. In particular, two isomers of the [HCo15Pd9C3(CO)38]2- nanocluster, referred as TP-Pd9 and Oh-Pd9, have been structurally characterized by single-crystal X-ray crystallography as their [NMe3(CH2Ph)]2[HCo15Pd9C3(CO)38]·CH2Cl2 (ca. 1:1 TP-Pd9 and Oh-Pd9 mixture), [NMe3(CH2Ph)]2[HCo15Pd9C3(CO)38]·2CH2Cl2 (mainly TP-Pd9), [NEt3(CH2Ph)]2[HCo15Pd9C3(CO)38]·CH2Cl2 (mainly TP-Pd9), [MePPh3]2[HCo15Pd9C3(CO)38]·2.5CH2Cl2 (mainly TP-Pd9), and [MePPh3]2[HCo15Pd9C3(CO)38] (Oh-Pd9) salts. The cluster core of TP-Pd9 is a tricapped trigonal prism, whereas this is a tricapped octahedron in Oh-Pd9. The presence in the solid state of the Oh-Pd9 or TP-Pd9 isomers depends on the cation employed and/or the number and type of co-crystallized solvent molecules. Often, mixtures of the two isomers, within the same single crystal or as mixtures of different crystals within the same crystallization batch, are obtained. Structural isomerism in organometallic nanoclusters is discussed and compared to that in Au-thiolate nanoclusters.

The reaction of [Ni6(CO)12]2– as a [NBu4]+ salt in CH2Cl2 with 0.8 equiv of PCl3 afforded [Ni14P2(CO)22]2–. In contrast, the reactions of [Ni6(CO)12]2– as a [NEt4]+ salt with 0.4–0.5 equiv of POCl3 afforded [Ni22–xP2(CO)29–x]4– (x = 0.84) or [Ni39P3(CO)44]6– by using CH3CN and thf as a solvent, respectively. Moreover, by using 0.7–0.9 mol of POCl3 per mole of [NEt4]2[Ni6(CO)12] both in CH3CN and thf, [Ni23–xP2(CO)30–x]4– (x = 0.82) was obtained together with [Ni22P6(CO)30]2– as a side product. [Ni23–xP2(CO)30–x]4– (x = 0.82) and [Ni22P6(CO)30]2– were separated owing to their different solubility in organic solvents. All the new molecular nickel phosphide carbonyl nanoclusters were structurally characterized through single crystal X-ray diffraction (SC-XRD) as [NBu4]2[Ni14P2(CO)22] (two different polymorphs, P21/n and C2/c), [NEt4]4[Ni23–xP2(CO)30–x]·CH3COCH3·solv (x = 0.82), [NEt4]2[Ni22P6(CO)30]·2thf, [NEt4]4[Ni22–xP2(CO)29–x]·2CH3COCH3( x = 0.84) and [NEt4]6[Ni39P3(CO)44]·C6H14·solv. The metal cores’ sizes of these clusters range from 0.59 to 1.10 nm, and their overall dimensions including the CO ligands are 1.16–1.63 nm. In this respect, they are comparable to ultrasmall metal nanoparticles, molecular nanoclusters, or atomically precise metal nanoparticles. The environment of the P atoms within these molecular Ni–P–CO nanoclusters displays a rich diversity, that is, Ni5P pentagonal pyramid, Ni7P monocapped trigonal prism, Ni8P bicapped trigonal prism, Ni9P monocapped square antiprism, Ni10P sphenocorona, Ni10P bicapped square antiprism, and Ni12P icosahedron., Five new molecular nickel phosphide carbonyl clusters have been obtained displaying overall sizes in the range 1.16−1.63 nm and very diverse environments for the phosphide atoms.