RESUMEN
The Schulze-Hardy rule is a well-established observation in colloid science (can be derived from the DLVO theory) that demonstrates the relationship between the critical coagulation concentration (CCC) of colloids and the valence of extra counterionic electrolytes (z), with a simple mathematical relationship of CCC≈z-6 . Here the Schulze-Hardy Rule is expanded to much smaller, nano-scaled soluble macroions in aqueous solution, by examining the stability of the macroions in the presence of additional electrolytes. The CCC values of the macroions follow the general trend of CCC≈z-n but the n value is significantly dependent on the surface charge density of the macroions, ranging from n=2 at very low surface charge density to n=6 at a high surface charge density. In addition, different cations with the same valence showed clear different impacts on the CCC values, with an interesting trend being connected to the Hofmeister series originally discovered in protein solutions.
RESUMEN
The SrII -centered 12-palladate(II) open-cube {SrPd12 (OAc)3 } has been systematically evolved by substitution of the three acetate ligands by a library of saturated carboxylic acids with increasing chain lengths leading to four novel polyoxopalladates(II) with the formula [SrPd12 O6 (OH)3 (PhAsO3 )6 (L)3 ]4- (SrPd12 L3 , L=Cn H2n+1 COO, n=2 to 5). These first examples of surfactant-type polyoxopalladates with a hydrophilic metal-oxo unit and three hydrophobic alkyl chains were characterized in the solid state (single-crystal XRD, FTIR, TGA), in solution (1 H, 13 Câ NMR spectroscopy), and in the gas phase (ESI-MS). The two polyanions SrPd12 L3 with chain lengths of 5 and 6 are the first examples of polyoxopalladates that are soluble and stable in organic media. The Na salts of the amphiphilic polyoxopalladates SrPd12 L3 were shown to self-assemble into "blackberry"-type spherical supramolecular structures in dilute solutions, of which an unusual "volcano"-shaped trend of assembly size versus solvent polarity is chiefly influenced by directional hydrogen bonding interactions.
RESUMEN
Three types of macroanion-countercation interactions in dilute solution, decided by the strength of electrostatic attraction and the change of hydration shells are reported: minor interaction between macroanions [MO8 Pd12 (SeO3 )8 ]6- (M=Zn2+ or Ni2+ ) and monovalent cations (Na+ , K+ , Rb+ , Cs+ ), leaving their hydration shells intact (solvent-separated ion-pairs); strong binding between macroanions and divalent cations (Sr2+ , Ba2+ ) to form solvent-shared ion-pairs with partial dehydration; very strong electrostatic attraction between macroanions and Y3+ ion with contact ion-pairs formation by severely breaking their original hydration shells and forming new ones. In addition, divalent cations can help the macroanions self-assemble into hollow spherical blackberry structures through counterion-mediated attraction, whereas macroanions with mono- or trivalent cations only stay as discrete ions due to either weak interaction or a small number of bound countercations.
RESUMEN
A series of nine [Sb7W36O133Ln3M2(OAc)(H2O)8](17-) heterometallic anions (Ln3M2; Ln=La-Gd, M=Co; Ln=Ce, M=Ni and Zn) have been obtained by reacting 3 d metal disubstituted Krebs-type tungstoantimonates(III) with early lanthanides. Their unique tetrameric structure contains a novel {MW9O33} capping unit formed by a planar {MW6O24} fragment to which three {WO2} groups are condensed to form a tungstate skeleton identical to that of a hypothetical trilacunary derivative of the É-Keggin cluster. It is shown, for the first time, that classical Anderson-Evans {MW6O24} anions can act as building blocks to construct purely inorganic large frameworks. Unprecedented reactivity in the outer ring of these disk-shaped species is also revealed. The Ln3M2 anions possess chirality owing to a {Sb4O4} cluster being encapsulated in left- or right-handed orientations. Their ability to self-associate in blackberry-type vesicles in solution has been assessed for the Ce3Co2 derivative.
Asunto(s)
Aniones/química , Cerio/química , Elementos de la Serie de los Lantanoides/química , Compuestos Organometálicos/química , Compuestos de Tungsteno/química , Cristalografía por Rayos XRESUMEN
The precise guidance to different ions across the biological channels is essential for many biological processes. An artificial nanopore system will facilitate the study of the ion-transport mechanism through nanosized channels and offer new views for designing nanodevices. Herein we reveal that a 2.5 nm-sized, fullerene-shaped molecular cluster Li48+m K12(OH)m [UO2(O2)(OH)]60-(H2O)n (m ≈ 20 and n ≈ 310) (U60) shows selective permeability to different alkali ions. The subnanometer pores on the water-ligand-rich surface of U60 are able to block Rb(+) and Cs(+) ions from passing through, while allowing Na(+) and K(+) ions, which possess larger hydrated sizes, to enter the interior space of U60. An interestingly high entropy gain during the binding process between U60 and alkali ions suggests that the hydration shells of Na(+)/K(+) and U60 are damaged during the interaction. The ion selectivity of U60 is greatly influenced by both the morphologies of the surface nanopores and the dynamics of the hydration shells.
RESUMEN
The self-assembly of semiglobular, positively charged poly(propyleneimine) (PPI) dendrimers with small monovalent counterions (e.g., Cl(-)) in water/acetone mixtures was investigated. We showed that PPI dendrimers can assemble into hollow, spherical, single-layered blackberry-type structures mediated by the presence of monovalent counterions. The effects on the assembly of changing the solvent polarity and adjusting the pH were further investigated to confirm the presence of electrostatic interactions and hydrogen bonding as the driving forces. Results showed that PPI dendrimers form stable, hollow spheres in 5-20% v/v acetone/water and that the size of the spheres decreases monotonically as the solvent polarity and/or the charge on the dendrimers (i.e., lower solution pH) increases. This is the first example to show that small monovalent counterions can trigger attraction among PPI dendrimers (or broadly defined polyelectrolytes) that is strong enough to bring them together to form large, stable supramolecular assemblies, which indicates that these organic macroions have similar solution behavior to more-well-defined inorganic molecular macroions.
RESUMEN
Two Keplerate-type macroions, [Mo(VI) 72 Fe(III) 30 O252 - (CH3 COO)12 {Mo2 O7 (H2 O)}2 {H2 Mo2 O8 (H2 O)}(H2 O)91 ]â ca. 150 H2 O= {Mo72 Fe30 } and [{Na(H2 O)12 }â{Mo(VI) 72 Cr(III) 30 O252 (CH3 COO)19 - (H2 O)94 }]â ca. 120 H2 O={Mo72 Cr30 }, with identical size and shape but different charge density, can self-assemble into spherical "blackberry"-like structures in aqueous solution by means of electrostatic interactions. These two macroanions can self-recognize each other and self-assemble into two separate types of homogeneous blackberries in their mixed dilute aqueous solution, in which they carry -7 and -5 net charges, respectively. Either adjusting the solution pH or raising temperature is expected to make the self-recognition more difficult, by making the charge densities of the two clusters closer, or by decreasing the activation energy barrier for the blackberry formation, respectively. Amazingly, the self-recognition behavior remains, as confirmed by dynamic and static light scattering, TEM, and energy dispersive spectroscopy techniques. The results prove that the self-recognition behavior of the macroions due to the long-range electrostatic interaction is universal and can be achieved when only minimum differences exist between two types of macroanions.
RESUMEN
The solution behavior of the two polyoxo-13-palladates(II) ([Pd(II) 13 As(V) 8 O34 (OH)6 ](8-) and [Pd(II) 13 (As(V) Ph)8 O32 ](6-) ) was studied in detail. We discovered that the countercation-mediated attraction is the driving force for their self-assembly into larger architectures. However, the presence of phenyl groups in the periphery of [Pd(II) 13 (As(V) Ph)8 O32 ](6-) results in an enhanced attraction among these polyanions through hydrophobic interactions, which leads to completely different trends of assembly size for these two very similar clusters when decreasing solvent polarity. An increase of assembly size with increasing solvent polarity was observed for [Pd(II) 13 (As(V) Ph)8 O32 ](6-) , whereas for [Pd(II) 13 As (V) 8 O34 (OH)6 ](8-) it was the opposite, due to the absence of hydrophobic interactions.
RESUMEN
Reaction of early lanthanides, GeO2 , and Na2 WO4 in a NaOAc buffer results in large crown-shaped polyoxometalates based on [Ln2 GeW10 O38 ](6-) subunits. By using Ni(2+) as a crystallizing agent, [NaâLn12 Ge6 W60 O228 (H2 O)24 ](35-) (NaâLn12 ) hexamers formed by alternating ß(1,5)/ß(1,8) subunits were obtained for Ln=Pr, Nd. The addition of K(+) led to a similar anion for Ln=Sm, namely, [KâSm12 Ge6 W60 O228 (H2 O)22 ](35-) (KâSm12 ) and [KâK7 Ln24 Ge12 W120 O444 (OH)12 (H2 O)64 ](52-) (KâLn24 ) dodecamers that consist of a central core identical to KâSm12 decorated with six external γ(3,4) subunits for Ln=Pr, Nd. These anions dissociate in water into hexameric cores and monomeric entities, as shown by ESI mass spectrometry. The former self-assemble into spherical, hollow, and single-layered blackberry-type structures with radii of approximately 75â nm, as monitored by laser light scattering (LLS) and TEM techniques. Analogous studies performed for KâNd24 in water/acetone mixtures show that the dodecamers remain stable and form in turn their own type of blackberries with sizes that increase from approximately 20 to 50â nm with increasing acetone content. This control over both the composition and size of the vesicle-like assemblies is achieved for the first time by modifying the architecture of the species that undergoes supramolecular association through the solvent polarity.
Asunto(s)
Germanio/química , Elementos de la Serie de los Lantanoides/química , Compuestos de Tungsteno/química , Aniones/química , Cristalización , Dimerización , Modelos Moleculares , Solventes , Agua/químicaRESUMEN
The research on chiral recognition and chiral selection is not only fundamental in resolving the puzzle of homochirality, but also instructive in chiral separation and stereoselective catalysis. Here we report the chiral recognition and chiral selection during the self-assembly process of two enantiomeric wheel-shaped macroanions, [Fe28(µ3-O)8(Tart)16(HCOO)24](20-) (Tart=D- or L-tartaric acid tetra-anion). The enantiomers are observed to remain self-sorted and self-assemble into their individual assemblies in their racemic mixture solution. The addition of chiral co-anions can selectively suppress the self-assembly process of the enantiomeric macroanions, which is further used to separate the two enantiomers from their mixtures on the basis of the size difference between the monomers and the assemblies. We believe that delicate long-range electrostatic interactions could be responsible for such high-level chiral recognition and selection.
Asunto(s)
Bario/química , Materiales Biomiméticos/química , Hierro/química , Tartratos/química , Aniones , Calcio/química , Catálisis , Cationes Bivalentes , Proteínas/química , Soluciones , Electricidad Estática , EstereoisomerismoRESUMEN
The hedgehog-shaped {Mo368} cluster shows unique electronic (extremely high extinction coefficient) and structural features, especially regarding its size, the high number of delocalized electrons which allows to measure the surface enhanced Raman scattering (SERS) spectrum and the option for coordination chemistry inside the cavity. Its relative instability in aqueous solution can be overcome by embedment in a hydrophobic shell of dimethyldioctadecylammonium cations. The resulting hybrid self-assembles into spherical vesicles in acetone-water mixtures, according to a process directed by hydrophobic-hydrophilic interactions. It also forms rather stable Langmuir monolayers while a second layer evolves under higher surface pressure, in accordance with a rather low alkyl surface density.
RESUMEN
Diamond nanocrystals were synthesized catalyst-free from nanoporous carbon at high pressure and high temperature (HPHT). The synthesized nanocrystals have tunable diameters between 50 and 200 nm. The nanocrystals are dispersible in organic solvents such as acetone and are isotropic in nature as seen by dynamic light scattering.
RESUMEN
The symmetry, structure and formation mechanism of the structurally self-complementary {Pd84} = [Pd84O42(PO4)42(CH3CO2)28](70-) wheel is explored. Not only does the symmetry give rise to a non-closest packed structure, the mechanism of the wheel formation is proposed to depend on the delicate balance between reaction conditions. We achieve the resolution of gigantic polyoxopalladate species through electrophoresis and size-exclusion chromatography, the latter has been used in conjunction with electrospray mass spectrometry to probe the formation of the ring, which was found to proceed by the stepwise aggregation of {Pd6}(-) = [Pd6O4(CH3CO2)2(PO4)3Na(6-n)H(n)](-) building blocks. Furthermore, the higher-order assembly of these clusters into hollow blackberry structures of around 50â nm has been observed using dynamic and static light scattering.
RESUMEN
An inorganic-organic hybrid surfactant with a hexavanadate cluster as the polar head group was designed and observed to assemble into micelle structures, which further spontaneously coagulate into a 1D anisotropic structure in aqueous solutions. Such a hierarchical self-assembly process is driven by the cooperation of varied noncovalent interactions, including hydrophobic, electrostatic, and hydrogen-bonding interactions. The hydrophobic interaction drives the quick formation of the micelle structure; electrostatic interactions involving counterions leads to the further coagulation of the micelles into larger assemblies. This process is similar to the crystallization process, but the specific counterions and the directional hydrogen bonding lead to the 1D growth of the final assemblies. Since most of the hexavanadates are exposed to the surface, the 1D assembly with nanoscale thickness is a highly efficient heterogeneous catalyst for the oxidation of organic sulfides with appreciable recyclability.
Asunto(s)
Compuestos de Tungsteno/química , Anisotropía , Catálisis , Cristalografía por Rayos X , Enlace de Hidrógeno , Modelos Moleculares , Estructura MolecularRESUMEN
POM and circumstance: Nanometer-sized polyoxometalates (POMs) bring a new direction to anion-templated supramolecular chemistry. The Keggin (left) and Dawson-type (right) polyoxoanions direct the assembly of giant metallomacrocycles through an array of weak hydrogen-bonding interactions. The concerted action of multiple hydrogen bonds keeps the templating guests embedded within the hosts, even in the solution state.
RESUMEN
A macroion, having anisotropic surface charge density distribution, shows unique self-assembly behaviour in polar solvents. Regular "blackberry"-like assemblies form in methanol-water mixtures due to counter-ion mediated attraction and the strong contribution of hydrogen bonding. However, rod-like assemblies form in acetone-water mixtures as the charge inhomogeneity effect overcomes the non-directional hydrogen bonding.
RESUMEN
Unique properties of the two giant wheel-shaped molybdenum-oxides of the type {Mo(154)}≡[{Mo(2)}{Mo(8)}{Mo(1)}](14) (1) and {Mo(176)}≡[{Mo(2)}{Mo(8)}{Mo(1)}](16) (2) that have the same building blocks either 14 or 16 times, respectively, are considered and show a "chemical adaptability" as a new phenomenon regarding the integration of a large number of appropriate cations and anions, for example, in form of the large "salt-like" {M(SO(4))}(16) rings (M = K(+), NH(4)(+)), while the two resulting {Mo(146)(K(SO(4)))(16)} (3) and {Mo(146)(NH(4)(SO(4)))(16)} (4) type hybrid compounds have the same shape as the parent ring structures. The chemical adaptability, which also allows the integration of anions and cations even at the same positions in the {Mo(4)O(6)}-type units of 1 and 2, is caused by easy changes in constitution by reorganisation and simultaneous release of (some) building blocks (one example: two opposite orientations of the same functional groups, that is, of H(2)O{Mo=O} (I) and O={Mo(H(2)O)} (II) are possible). Whereas Cu(2+) in [(H(4)Cu(II)(5))Mo(V)(28)Mo(VI)(114)O(432)(H(2)O)(58)](26-) (5 a) is simply coordinated to two parent O(2-) ions of {Mo(4)O(6)} and to two fragments of typeâ II, the SO(4)(2-) integration in 3 and 4 occurs through the substitution of two oxo ligands of {Mo(4)O(6)} as well as two H(2)O ligands of fragmentâ I. Complexes 3 and now 4 were characterised by different physical methods, for example, solutions of 4 in DMSO with sophisticated NMR spectroscopy (EXSY, DOSY and HSQC). The NH(4)(+) ions integrated in the cluster anion of 4 "communicate" with those in solution in the sense that the related H(+) ion exchange is in equilibrium. The important message: the reported "chemical adaptability" has its formal counterpart in solutions of "molybdates", which can form unique dynamic libraries containing constituents/building blocks that may form and break reversibly and can lead to the isolation of a variety of giant clusters with unusual properties.