Experimental verification of the formation mechanism for pillar arrays in nanofilms subject to large thermal gradients

The free surface of molten nanofilms is known to undergo spontaneous formation of periodic protrusions when exposed to a large transverse thermal gradient. Early time measurements of the array pitch and growth rate in polymer melts confirm a formation process based on a long wavelength thermocapillary instability and not electrostatic attraction or acoustic phonon driven growth as previously believed. We find excellent agreement with theoretical predictions provided the nanofilm out-of-plane thermal conductivity is several times larger than bulk, an enhancement suggestive of polymer chain alignment.     

Das Atomgewicht des Radiums

Ohne Zusammenfassung     

Eine Lampe zur Erhitzung langer Gegenst?nde

Ohne Zusammenfassung     

Rapidly Adaptive All-covalent Nanoparticle Surface Engineering

Emerging nanotechnologies demand the manipulation of nanoscale components with the same predictability and programmability as is taken for granted in molecular synthetic methodologies. Yet installing appropriately reactive chemical functionality on nanomaterial surfaces has previously entailed compromises in terms of reactivity scope, functionalization density, or both. Here, we introduce an idealized dynamic covalent nanoparticle building block for divergent and adaptive post-synthesis modification of colloidal nanomaterials. Acetal-protected monolayer-stabilized gold nanoparticles are prepared via operationally simple protocols and are stable to long-term storage. Tunable surface densities of reactive aldehyde functionalities are revealed on-demand, leading to a wide range of adaptive surface engineering options from one nanoscale synthon. Analytically tractable with molecular precision, interfacial reaction kinetics and dynamic surface constitutions can be probed in situ at the ensemble level. High functionalization densities combined with rapid equilibration kinetics enable environmentally adaptive surface constitutions and rapid nanoparticle property switching in response to simple chemical effectors.     

Synthesis of alpha-P-modified nucleoside diphosphates with ethylenediamine

This report describes a one-pot synthesis of alpha-P-borano-, alpha-P-thio-, and alpha-P-seleno-modified nucleoside diphosphate analogues that are otherwise difficult to obtain. The key step involves the intramolecular nucleophilic attack by an amino group in 5 to remove the gamma-phosphate. The absolute configurations of P-diastereomers were confirmed by analysis of their 1H NMR. Affinity studies revealed that the nucleoside boranodiphosphates are potentially useful in antiviral research.     

Cross-sections for deuteron photo-disintegration from 74 to 241 MeV

Recent measurements of the differential cross-sections for deuteron photo-disintegration have been extended to lower photon energies at selected c.m. angles. The new results agree with earlier values from this laboratory and confirm the large discrepancy with data from Bonn and Orsay noted in the 100–250 MeV energy-range. They are in good agreement with the results of theoretical calculations including isobar configurations and meson-exchange currents below 150 MeV.     

A novel undecametallic iron(III) cluster with an S = (11)/(2) spin ground state

The reaction of [NEt(4)](2)[Fe(2)OCl(6)] with sodium benzoate, 4,6-dimethyl-2-hydroxypyrimidine (dmhp), and 1,1,1-tris(hydroxymethyl)ethane (H(3)thme) gives the undecametallic compound [NEt(4)][Fe(11)O(4)(O(2)CPh)(10)(thme)(4)(dmhp)(2)Cl(4)]. X-ray crystallography, EPR spectroscopy, bulk magnetic susceptibility studies, and low-temperature single-crystal magnetic measurements were used to characterize the compound. Magnetic measurements indicate an S = (11)/(2) ground state with the parameters g = 2.03 and D = -0.46 cm(-)(1). Single-crystal magnetic studies show hysteresis of molecular origin at T < 1.2 K with fast quantum mechanical tunneling at zero field.     

Synthesis, structure and magnetic properties of a trinuclear [Mn(III)Mn(II)2] single-molecule magnet

Ferromagnetic exchange between the three Mn ions in the complex [Mn3(Hcht)2(bpy)4](ClO4)3 leads to a spin ground state of S = 7; single crystal studies reveal the temperature and sweep rate dependent hysteresis loops expected for a single-molecule magnet.