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2 protocols using zinc chloride

1

Synthesis of Colloidal Metal Chalcogenide Nanocrystals

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All anhydrous chemicals were stored in a nitrogen-filled glovebox. Indium acetate (In[OAc]3, anhydrous, 99.9%) and zinc oxide (ZnO, 99.9%) were purchased from Sigma-Aldrich. Indium chloride (InCl3, anhydrous, 2N), gallium chloride (GaCl3, 5N), and gallium nitrate (Ga[NO3]3·nH2O) were purchased from Mitsuwa Chemical Co., Ltd. OA (85%), tri-n-butyl phosphine (TBP, >95%), TOP (>85%), and zinc chloride (ZnCl2, 98.0%) were obtained from Tokyo Chemical Industry. Silver acetate (Ag[OAc], anhydrous, 99.9%), sodium N,N′-diethyldithiocarbamate (NaDDTC, 92.0%), hexane (anhydrous, 96%), and toluene (anhydrous, 99.8%) were purchased from Fujifilm Wako Pure Chemical. All chemicals were used without further purification. OLA was purchased from Fujifilm Wako Pure Chemical and was purified by vacuum distillation in the presence of calcium hydride.
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2

Fluorescent Sensor Synthesis and Characterization

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1-Nitroso-2-naphthol, zinc chloride, (2-bromoethyl)benzene, 2,3,3-trimethylindolenine,
and triethylamine were purchased from Tokyo Chemical Industry (TCI).
Tetrahydrofuran, acetonitrile, dichloromethane, and ethanol were obtained
from Honeywell Burdick & Jackson (B&J). Metal ions including
Na+, K+, Mg2+, Ca2+, Sr2+, Ba2+, Sn2+, Pb2+, Cr3+, Mn2+, Fe2+, Fe3+, Co2+, Ni2+, Cu2+, Zn2+, Cd2+, and Hg2+ were obtained from Sigma-Aldrich as
chloride salts. All reagents were of analytical grade and used as
received unless stated otherwise. Deionized water (DI) was used for
all experiments. Analytical thin-layer chromatography (TLC) was performed
on Kieselgel F254 pre-coated aluminum TLC plates obtained
from EM Science. Visualization was performed with a 254 nm ultraviolet
lamp. Column chromatography was carried out with Merck silica gel
60 (230–400 mesh ASTM). UV/vis absorption spectra were measured
on a Shimadzu (UV-1800) spectrophotometer at ambient temperature.
The path length of a quartz cell was 1 cm. 1H NMR (500
MHz) and 13C NMR (125 MHz) spectra with entire proton decoupling
were recorded on a Bruker AVANCE 500 NMR spectrometer, and chemical
shifts in ppm were quoted relative to the residual signals of deuterated
solvents. High-resolution mass spectra were recorded using a Bruker
micrOTOF mass spectrometer (ESI-TOF) and reported with ion mass/charge
(m/z) ratios as values in atomic mass units.
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