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Au wafers

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Au wafers are thin, circular discs made of gold that are used as a substrate material in various laboratory and industrial applications. They provide a stable and uniform surface for the deposition of thin films or the growth of materials. Au wafers are primarily used in research, development, and manufacturing processes that involve surface analysis, thin film deposition, and materials characterization.

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Lab products found in correlation

6 mercaptohexanoic acid, by Merck Group (2 mentions) Adamantane, by Merck Group (1 mentions) Styrene oxide, by Merck Group (1 mentions) Benzaldehyde, by Merck Group (1 mentions) Benzyl alcohol, by Merck Group (1 mentions) Styrene, by Merck Group (1 mentions) Cyclohexanol, by Merck Group (1 mentions)

3 protocols using au wafers

1

Synthesis, Characterization, and Applications

Cited 1 time
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1-Azidoundecane-11-thiol and Hemin-yne were synthesized following the reported procedure29 (link)69 (link). 6-Mercaptohexanoic acid was purchased from Sigma Aldrich. Di-sodium hydrogenphosphate dihydrate (Na2HPO4. 2H2O) was purchased from Merck. 2, 6-lutidine was purchased from Avra Synthesis Pvt. Ltd. These chemicals were used without further purification. Au wafers were purchased from Platypus Technologies (1,000 Å of Au on 50 Å of Ti adhesion layer on top of a Si(III) surface). Transparent Au wafers (100 Å of Au on 10 Å of Ti) were purchased from Phasis, Switzerland. Au and Ag discs for the RRDE and SERRS experiments, respectively, were purchased from Pine Instruments, USA. The Mb mutants were prepared as reported in the literature7 (link)30 . Analysis of the components of the rR spectrum was done by using Lorenztian line shape of peak fit software.
Mukherjee S., Mukherjee A., Bhagi-Damodaran A., Mukherjee M., Lu Y, & Dey A. (2015). A biosynthetic model of cytochrome c oxidase as an electrocatalyst for oxygen reduction. Nature Communications, 6, 8467.
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2

Synthesis and Characterization of Thiol-Modified Compounds

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1-Azidoundecane-11-thiol and Hemin-yne were synthesized following the reported procedure.15 ,16 (link) 6-Mercaptohexanoic acid was purchased from Sigma-Aldrich. Disodium hydrogen phosphate dihydrate (Na2HPO4.2H2O) was purchased from Merck. 2,6-Lutidine was purchased from Avra Synthesis Pvt., Ltd. These chemicals were used without further purification. Au wafers were purchased from Platypus Technologies (1000 Å of Au on 50 Å of Ti adhesion layer on top of a Si(III) surface). Au and Ag discs for the Rotating Ring Disc Electrochemistry (RRDE) and Surface Enhanced Resonance Raman Spectroscopy (SERRS) experiments, respectively, were purchased from Pine Instruments, U.S.A. The Mb mutants were prepared as reported in the literature.17 ,18 Analysis of the components of the rR spectrum were done by using Lorenztian line shape of peak fit software.
Mukherjee S., Mukherjee M., Mukherjee A., Bhagi-Damodaran A., Lu Y, & Dey A. (2018). O2 Reduction by Biosynthetic Models of Cytochrome c Oxidase: Insights into Role of Proton Transfer Residues from Perturbed Active Sites Models of CcO. ACS catalysis, 8(9), 8915-8924.
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3

Synthesis and Characterization of Picket Fence Iron Porphyrin

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All
reagents were of the
highest grade commercially available and were used without further
purification. Octanethiol (C8SH), butanethiol (C4SH), potassium hexafluorophosphate (KPF6), benzyl alcohol,
benzaldehyde, styrene, styrene oxide, adamantane, and phenylacetaldehyde
were purchased from Sigma-Aldrich. Disodium hydrogen phosphate dihydrate
(Na2HPO4·2H2O), cyclohexane,
and cyclohexanol were purchased from Merck. Triethylamine (Et3N), toluene, ethylbenzene, and acetophenone were purchased
from Spectrochem India Ltd. Au wafers were purchased from Platypus
Technologies (1000 Å of Au on 50 Å of Ti adhesion layer
on top of a Si(III) surface). The picket fence iron porphyrin was
synthesized and characterized following past literature reports.97 (link)
Mukherjee M, & Dey A. (2019). Electron Transfer Control of Reductase versus Monooxygenase: Catalytic C–H Bond Hydroxylation and Alkene Epoxidation by Molecular Oxygen. ACS Central Science, 5(4), 671-682.
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