Ultra-thin dendrimer films are effective resists for high-resolution lithography using a scanning probe. The authors describe dendritic monolayer formation via covalent attachment to a silicon wafer surface and the field-enhanced oxidation of the dendrimer monolayers using scanning probe lithography to create features with dimensions less than 60 nm. Poly-(benzyl ether) dendrimers, terminated with either benzyl or tert-butyldiphenylsilyl ether groups, were used because of their relative ease of preparation and derivatization.
The facile one-phase synthesis of N-heterocyclic carbene-stabilized gold nanoparticles (NHC-AuNP) by reduction of NHC-gold(I) complexes and their self-assembly into 3D superlattices is presented.
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
During the past decade, the use of Au(I) complexes for the catalytic activation of C-C π-bonds has been investigated intensely. Over this time period, the development of homogeneous gold catalysis has been extraordinarily rapid and has yielded a host of mild and selective methods for the formation of carbon-carbon and carbon-heteroatom bonds. The facile formation of new bonds facilitated by gold naturally led to efforts toward rendering these transformations enantioselective. In this Account, we survey the development of catalysts and ligands for enantioselective gold catalysis by our research group as well as related work by others. We also discuss some of our strategies to address the challenges of enantioselective gold(I) catalysis. Early on, our work with enantioselective gold-catalyzed transformations focused on bis(phosphinegold) complexes derived from axially chiral scaffolds. Although these complexes were highly successful in some reactions like cyclopropanation, the careful choice of the weakly coordinating ligand (or counterion) was necessary to obtain high levels of enantioselectivity for the case of allene hydroamination. These counterion effects led us to use the anion itself as a source of chirality, which was successful in the case of allene hydroalkoxylation. In general, these tactics enhance the steric influence around the reactive gold center beyond the two-coordinate ligand environment. The use of binuclear complexes allowed us to use the second gold center and its associated ligand (or counterion) to exert a further steric influence. In a similar vein, we employed a chiral anion (in place of or in addition to a chiral ligand) to move the chiral information closer to the reactive center. In order to expand the scope of reactions amenable to enantioselective gold catalysis to cycloadditions and other carbocyclization processes, we also developed a new class of mononuclear phosphite and phosphoramidite ligands to supplement the previously widely utilized phosphines. However, we needed to judiciously design the steric environment to create "walls" that enclose the gold center. We also successfully applied these same considerations to the development of binuclear carbene ligands for gold. Finally, we describe the design of bifunctional urea-monophosphine ligands used in a gold-catalyzed three-component coupling.
Abstract : The Ethane architecture, developed at Stanford University, demonstrated that a novel approach to building secure networks could support superior low-level security and flexible policy-based control over individual flows. However, Ethane only provided operators with a single function: policy-based access control. Moreover, Ethane's policy was expressed in a language that did not have a rigorous logical foundation. Almost a year of subsequent work, reported on here, extended Ethane to address these two shortcomings. First, the Ethane architecture was evolved from Ethane's narrowly targeted design to a fully general network operating system called NOX, which provides users with full-blown programmatic interface. Second, the policy language has evolved from the Ethane's primitive pol-eth to a much more powerful and rigorously analyzed Flow-Based Security Language (FSL). This report describes these two advances.
An entry from the Cambridge Structural Database, the world’s repository for small molecule crystal structures. The entry contains experimental data from a crystal diffraction study. The deposited dataset for this entry is freely available from the CCDC and typically includes 3D coordinates, cell parameters, space group, experimental conditions and quality measures.
This analysis indicates that tiotropium is associated with lower rates of AEs, SAEs, and similar rates of FAEs than placebo when delivered via HandiHaler(®) or Respimat(®) (overall and separately) in patients with COPD.
Recent advances in computer systems allow the electroencephalogram (EEG) to be recorded using a large number of channels, with a high sampling rate, and over a long period of time. As a result, storage of the acquired data has become a major problem in many practical systems. The authors investigate this problem and provide a procedure for the specification of three critical parameters: the gain of the amplifier, the sampling rate, and the order of the analog filter. This design achieves high-efficiency for the use of the computer resources, while maintaining the required precision for accurate analysis of the EEG data.< <ETX xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">></ETX>