Synthesis, Electrochemistry, and Excited-State Properties of Three Ru(II) Quaterpyridine Complexes.

The complexes [Ru(qpy)LL'](2+) (qpy = 2,2':6',2″:6″,2‴-quaterpyridine), with 1: L = acetonitrile, L'= chloride; 2: L = L'= acetonitrile; and 3: L = L'= vinylpyridine, have been prepared from [Ru(qpy) (Cl)2]. Their absorption spectra in CH3CN exhibit broad metal-to-ligand charge transfer (MLCT) absorptions arising from overlapping (1)A1 → (1)MLCT transitions. Photoluminescence is not observed at room temperature, but all three are weakly emissive in 4:1 ethanol/methanol glasses at 77 K with broad, featureless emissions observed between 600 and 1000 nm consistent with MLCT phosphorescence.

Charge-Transfer Effects in Ligand Exchange Reactions of Au25 Monolayer-Protected Clusters.

Reported here are second-order rate constants of associative ligand exchanges of Au25L18 nanoparticles (L = phenylethanethiolate) of various charge states, measured by proton nuclear magnetic resonance at room temperature and below. Differences in second-order rate constants (M(-1) s(-1)) of ligand exchange (positive clusters ∼1.9 × 10(-5) versus negative ones ∼1.

Temperature dependence of solid-state electron exchanges of mixed-valent ferrocenated Au monolayer-protected clusters.

Electron transfers (ETs) in mixed-valent ferrocene/ferrocenium materials are ordinarily facile. In contrast, the presence of ~1:1 mixed-valent ferrocenated thiolates in the organothiolate ligand shells of <2 nm diameter Au225, Au144, and Au25 monolayer-protected clusters (MPCs) exerts a retarding effect on ET between them at and below room temperature. Near room temperature, in dry samples, bimolecular rate constants for ET between organothiolate-ligated MPCs are diminished by the addition of ferrocenated ligands to their ligand shells.

Solution voltammetry of 4 nm magnetite iron oxide nanoparticles.

The voltammetry of solution-dispersed magnetite iron oxide Fe3O4 nanoparticles is described. Their currents are controlled by nanoparticle transport rates, as shown with potential step chronoamperometry and rotated disk voltammetry. In pH 2 citrate buffer with added NaClO4 electrolyte, solution cyclic voltammetry of these nanoparticles (average diameter 4.

Electronic conductivity of films of electroflocculated 2 nm iridium oxide nanoparticles.

The electronic conductivity of films of iridium oxide (IrO(x)) composed of ca. 2 nm nanoparticles (NPs) is strongly dependent on the film oxidation state. The Ir(IV)O(x) NPs can be electrochemically converted to several oxidation states, ranging from Ir(III) to Ir(V) oxides.

Formation of iridium(IV) oxide (IrOX) films by electroflocculation.

Films of iridium(IV) oxide nanoparticles (IrOX NPs) become deposited on electrodes from nanoparticle solutions when potentials sufficient to initiate water oxidation are applied. Evidence is given that the film-forming mechanism is nanoparticle precipitation. Following an induction period during which a significant amount of charge is passed, the NPs begin to deposit as islands.

Kinetics and low temperature studies of electron transfers in films of small (<2 nm) Au monolayer protected clusters.

This work examines the temperature dependence of electron transfer (ET) kinetics in solid-state films of mixed-valent states of monodisperse, small (<2 nm) Au monolayer protected clusters (MPCs). The mixed valent MPC films, coated on interdigitated array electrodes, are Au25(SR)18(0/1-), Au25(SR)18(1+/0), and Au144(SR)60(1+/0), where SR = hexanethiolate for Au144 and phenylethanethiolate for Au25. Near room temperature and for ca.

Synthesis and electrochemistry of 6 nm ferrocenated indium-tin oxide nanoparticles.

Indium-tin oxide (ITO) nanoparticles, 6.1 ± 0.8 nm in diameter, were synthesized using a hot injection method.

Electron transfer dynamics of iridium oxide nanoparticles attached to electrodes by self-assembled monolayers.

Self-assembled monolayers (SAMs) of carboxylated alkanethiolates (-S(CH(2))(n-1)CO(2)(-)) on flat gold electrode surfaces are used to tether small (ca. 2 nm d.) iridium(IV) oxide nanoparticles (Ir(IV)O(X) NPs) to the electrode.

Mass spectrometry of ligand exchange chelation of the nanoparticle [Au25(SCH2CH2C6H5)18]1- by CH3C6H3(SH)2.

Mass spectrally detected products of ligand exchange reactions of the nanoparticle [Au25(SC2H4C6H5)18](1-), (abbrev. Au25(SC2Ph)18), where the dithiol is toluene-3,4-dithiol, CH3C6H3(SH)2, include nanoparticles containing both doubly (bidentate, or chelating) and singly bonded dithiol. The bidentate binding displaces two of the original -SC2Ph ligands, and singly bonded dithiol displaces one -SC2Ph ligand, while maintaining, for mass spectrally detected species, occupancy of 18 ligation sites.

Synthesis of monodisperse [Oct4N(+)][Au25(SR)18(-)] nanoparticles, with some mechanistic observations.

A single phase (THF) synthesis of monodisperse [Oct(4)N(+)][Au(25)(SR)(18)(-)] nanoparticles is described that yields insights into pathways by which it is formed from initially produced larger nanoparticles. Including the Oct(4)N(+)Br(-) salt in a reported single phase synthetic procedure enables production of reduced nanoparticles having a fully occupied HOMO molecular energy level (Au(25)(SR)(18)(-), as opposed to a partially oxidized state, Au(25)(SR)(18)(0)). The revised synthesis accommodates several (but not all) different thiolate ligands.

An editor's view of analytical chemistry (the Discipline).

The author recounts progress observed in analytical chemistry (the discipline) from the vantage point of a 20-year editor of Analytical Chemistry (the journal). The recounting draws liberally from the journal's monthly editorials. A complete listing of the editorials can be found in Supplemental Material .

The story of a monodisperse gold nanoparticle: Au25L18.

Au nanoparticles (NPs) with protecting organothiolate ligands and core diameters smaller than 2 nm are interesting materials because their size-dependent properties range from metal-like to molecule-like. This Account focuses on the most thoroughly investigated of these NPs, Au(25)L(18). Future advances in nanocluster catalysis and electronic miniaturization and biological applications such as drug delivery will depend on a thorough understanding of nanoscale materials in which molecule-like characteristics appear.

Ferrocenated au nanoparticle monolayer adsorption on self-assembled monolayer-coated electrodes.

The robust, irreversible adsorption of omega-ferrocene hexanethiolate-protected gold nanoparticles (composition ca. {Au(225)(SC6Fc)(43)}) on electrodes provides an opportunity to investigate their submonolayer and monolayer films in nanoparticle-free solutions. Observations of nanoparticle adsorption on unmodified electrodes are extended here to Au electrodes having more explicitly controlled surfaces, namely self-assembled monolayers (SAMs) of alkanethiolates with omega-sulfonate, carboxylate, and methyl termini, and in different Bu(4)N(+)X(-) electrolyte (X(-) = C(7)H(7)SO(3)(-), ClO(4)(-), CF(3)SO(3)(-), PF(6)(-), NO(3)(-)) solutions in CH(2)Cl(2).

Interfacial ion transfers between a monolayer phase of cationic Au nanoparticles and contacting organic solvent.

The highly cationic nanoparticle [Au(225)(TEA-thiolate(+))(22)(SC6Fc)(9)] adsorbs so strongly on Pt electrodes from CH(3)CN/Bu(4)NClO(4) electrolyte solutions that films comprised of 1-2 monolayers of nanoparticles can be transferred to nanoparticle-free electrolyte solutions without desorption and ferrocene voltammetry stably observed. (TEA-thiolate(+) = -S(CH(2))(11)N(CH(2)CH(3))(3)(+); SC6Fc = S(CH(2))(6)-ferrocene; Fc = ferrocene). The Fc(+/0) redox couple's voltammetry is used to detect the adsorption.

Electrospray ionization mass spectrometry of intrinsically cationized nanoparticles, [Au(144/146)(SC(11)H(22)N(CH(2)CH(3))(3)(+))(x)(S(CH(2))(5)CH(3))(y)](x+).

Electrospray ionization triple-quadrupole mass spectrometry of ca. 1.6 nm diameter thiolate-protected gold nanoparticles has been achieved at higher resolution than in previous reports.

Electrogenerated IrO(x) nanoparticles as dissolved redox catalysts for water oxidation.

We describe the first example of redox catalysis using a dissolved electroactive nanoparticle, based on the oxidation of water by electrogenerated IrO(x) nanoparticles containing Ir(VI) states, in pH 13 solutions of 1.6 +/- 0.6 nm (dia.

Tandem mass spectrometry of thiolate-protected Au nanoparticles Na(x)Au25(SC2H4Ph)(18-y)(S(C2H4O)5CH3)(y).

We report the first collision-induced dissociation tandem mass spectrometry (CID MS/MS) of a thiolate-protected Au nanoparticle that has a crystallographically determined structure. CID spectra assert that dissociation pathways for the mixed monolayer Na(x)Au(25)(SC(2)H(4)Ph)(18-y)(S(C(2)H(4)O)(5)CH(3))(y) centrally involve the semi-ring Au(2)L(3) coordination (L = some combination of the two thiolate ligands) that constitutes the nanoparticle's protecting structure. The data additionally confirm charge state assignments in the mass spectra.

Gold nanoparticles: past, present, and future.

This perspective reviews recent developments in the synthesis, electrochemistry, and optical properties of gold nanoparticles, with emphasis on papers initiating the developments and with an eye to their consequences. Key aspects of Au nanoparticle synthesis have included the two-phase synthesis of thiolated nanoparticles, the sequestration and reduction of Au salts within dendrimers, the controlled growth of larger particles of well-defined shapes via the seeded approach, and the assembling of a variety of nanoparticle networks and nanostructures. The electrochemistry of thiolated Au nanoparticles is systemized as regions of bulk-continuum voltammetry, voltammetry reflective of quantized double-layer charging, and molecule-like voltammetry reflective of molecular energy gaps.

Mass spectrometry of small bimetal monolayer-protected clusters.

Monolayer-protected clusters were prepared by procedures like those yielding Au25L18 (where L=-SCH2CH2Ph=-SC2Ph) but using, instead, mixtures of Au and Pd salts, as starting materials, with the intent of creating and characterizing Au25-xMxL18 clusters. Isolation of small nanoparticle product followed by partial ligand exchange to introduce thiolated poly(ethylene glycol) (SPEG=-S(CH2CH2O)5CH3) into the nanoparticle ligand shell enabled characterization of the Au25-xMxL18 content by positive mode electrospray ionization mass spectrometry (ESI-MS). For synthetic feed mole ratios of Au:Pd of 9:1 and 13:12, electrospray spectra of the PEGylated MPCs showed that the reaction and isolation produce a mixture of Au25(SC2Ph)18 and a mono-Pd nanoparticle Au24Pd(SC2Ph)18.

Voltammetry and redox charge storage capacity of ferrocene-functionalized silica nanoparticles.

We describe the electrochemistry of 15 nm diameter silica nanoparticles densely functionalized with ferrocene (FcSiO(2)) through siloxane couplings. Each nanoparticle bears approximately 600 Fc sites, as measured by potentiometric titration (590 Fc) and diffusion-controlled voltammetry (585 Fc) and estimated by XPS (630 Fc). The nanoparticle ferrocene coverage amounts to ca.