17 research outputs found
Single Molecular Bridging of Au Nanogap Using Aryl Halide Molecules
Single molecular junctions of benzene
dihalide molecules (<i>para</i>-Xā(C<sub>6</sub>H<sub>4</sub>)āX, X =
Cl, Br, I) binding to Au electrodes were systematically studied by
using the scanning tunneling microscopy break junction (STM-BJ) technique.
The STM-BJ characterization revealed that the single molecular junction
was formed only with 1,4-diiodobenzene, which was due to its ability
to form particularly stable halogen bonds with Au electrodes for the
iodide anchoring group. The conductance and strength of the metalāmolecule
bond of the single 1,4-diiodobenzene molecular junction were compared
with that of 1,4-benzenediamine (<i>para-</i>H<sub>2</sub>Nā(C<sub>6</sub>H<sub>4</sub>)āNH<sub>2</sub>). The
conductance of a single 1,4-diiodobenzene molecular junction was 3.6
Ć 10<sup>ā4</sup> <i>G</i><sub>0</sub> (<i>G</i><sub>0</sub> = 2e<sup>2</sup>/h), which was smaller than
1 Ć 10<sup>ā2</sup> <i>G</i><sub>0</sub> measured
for 1,4-benzenediamine. The distances to break single molecular junctions
were 0.05 and 0.03 nm for single 1,4-diiodobenzene and 1,4-benzenediamine
molecular junctions, respectively. The longer breakdown distance of
the single 1,4-diiodobenzene molecular junctions indicated that the
AuāI bond was stronger than that of the AuāNH<sub>2</sub> bond. The present work demonstrates that an iodide group can be
utilized as an anchoring group for the single molecular junction
Active Palladium Colloids via Palladacycle Degradation as Efficient Catalysts for Oxidative Homocoupling and Cross-Coupling of Aryl Boronic Acids
Active palladium colloids formed
upon degradation of a palladacyclic
complex (HerrmannāBeller <b>1</b>) have been isolated
for the first time and thoroughly characterized with techniques such
as transmission electron microscopy (TEM), high-resolution TEM, X-ray
photoelectron spectroscopy (XPS), and extended X-ray absorption fine
structure spectroscopy. The synthesized palladium colloids have been
utilized as efficient catalysts for the oxidative homocoupling of
aryl boronic acids. Cross-coupling of two different aryl boronic acids
has also been made possible using these active palladium colloids.
This is the first report of this kind of coupling between aryl boronic
acids
High-Yielding One-Pot Synthesis of Glucose from Cellulose Using Simple Activated Carbons and Trace Hydrochloric Acid
High-yielding one-pot synthesis of
glucose from cellulose and pentoses/hexoses
from real biomass is achieved by using simple activated carbons and
0.012% HCl in water. Ball-milling cellulose and the carbon together
created good physical contact between the solid substrate and solid
catalyst before the reaction, selectively and drastically improving
the depolymerization rate of cellulose to oligomers. Thus, our methodology
overcomes a major obstacle in this type of reaction, namely, that
the collision between a solid catalyst and a solid substrate is limited.
Mechanistic studies have suggested that the active sites of the carbons
are weakly acidic functional groups, in which vicinal carboxylic and
phenolic groups synergistically work for the hydrolysis reaction
Percentages of post larvae on pepsin and trypsin treated FD HCl-ex of <i>C. gigas</i> SC.
<p>Shaded and open boxes represent pepsin and trypsin treated experiments, respectively. Data are means of 9 replicates and error bars represent standard deviations (SD). Lines connected groups that were compared using Wald test. Asterisks * indicate significantly different groups (p<0.05).</p
SDS-PAGE gel image of <i>C. gigas</i> FD HCl-ex, F1 (fraction 1) and F2 (fraction 2) stained with Stains-all.
<p>SDS-PAGE was performed on 10% polyacrylamide gels; 10 Āµg protein content was loaded in each lane. M indicates the molecular weight markers. Molecular weights were estimated using the molecular weight marker āBroad Rangeā (BIORAD).</p
ANOVA result of the effect of species and amount of SC on <i>C. gigas</i> larval settlement.
<p><sup></sup> Statistics of the quasi-binomial GLM applied to the output for dependent variable larval settlement. Species refers to the 11 species of SC tested; amount refers to the weight of SC.</p
Percentages of post larvae that settled on SC of the different species of mollusks.
<p>Closed squares are means of 6 to 30 replicates and error bars represent standard deviation (SD). Letters indicate results of the post hoc Tukey HSD test of activities within species at 0, 10, 50 and 100 mg. Values connected by the same letter are not significantly different (pā„0.05).</p
Percentages of post larvae on PNGase F and TFMS treated FD HCl-ex of <i>C. gigas</i> SC.
<p>Boxes with slanting lines indicate post larvae (%) settled on FD HCl-ex 100 mg SC eq subjected to the same treatment procedure but without trypsin. Data are means of 9 replicates and error bars represent standard deviations (SD). Lines connected groups that were compared using Wald test. Asterisks * indicate significantly different groups (p<0.05).</p
Taxonomy of the 11 species of mollusks used as specimens.
<p>Taxonomy of the 11 species of mollusks used as specimens.</p
Percentages of post larvae on <i>C. gigas</i> SC that were heated at different temperatures (A), and treated with antibiotic solutions (B).
<p>A: Boxes with slanting lines and shading indicate results of heat treatment experiments of 50 mg SC and 500 mg SC, respectively. x indicates no data. B: blank boxes indicate the antibiotic treatment experiment of 50 mg SC. 1ABā=āstreptomycin sulphate 20 mg L<sup>ā1</sup>, penicillin G 10 mg L<sup>ā1</sup>, neomycin 2 mg L<sup>ā1</sup>, and kanamycin 10 mg L<sup>ā1</sup>, and 10ABā=ā1AB concentration increased tenfold. Data are means of 6 to 9 replicates and error bars represent standard deviations (SD). Lowercase and uppercase letters indicate results of the post hoc Tukey HSD test on heat and antibiotic treatments, respectively. Groups connected by the same letter are not significantly different (pā„0.05).</p