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Chns o analyzer 2400ii

Manufactured by PerkinElmer
Sourced in United States

The CHNS/O Analyzer 2400II is a laboratory instrument used for the elemental analysis of organic and inorganic materials. It can accurately determine the carbon, hydrogen, nitrogen, sulfur, and oxygen content of a sample.

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2 protocols using chns o analyzer 2400ii

1

Synthesis and Characterization of Catalytic Compounds

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All solvents
used for the synthesis of the ligand and catalytic reaction (THF,
toluene, CH2Cl2, and MeCN) were purified over
a Glass Contour Solvent Dispending System under an Ar atmosphere.
Other reagents of the highest grade that were commercially available
were used without further purification. Atomic absorption analysis
was performed on a Shimadzu AA-6200. Elemental analysis was performed
on a Perkin-Elmer CHNS/O Analyzer 2400II. GC analysis was performed
on a Shimadzu GC2010 gas chromatograph with an Rtx-5 column (Restek,
length = 30 m, i.d. = 0.25 mm, and thickness = 0.25 μm). IR
spectra were recorded on a JASCO FT/IR 4200 spectrometer. NMR spectra
were recorded on a JEOL ECA-600 spectrometer. UV–vis spectra
of solution samples were recorded on a JASCO V650 spectrometer, and
solid reflectance spectra were recorded on the same instrument with
a PIN-757 integrating sphere attachment for solid. Nitrogen sorption
studies were performed at liquid nitrogen temperature (77 K) using
Micromeritics TriStar 3000. Before the adsorption experiments, the
samples were outgassed under reduced pressure for 3 h at 333 K.
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2

Characterization of Cobalt(II) Complexes

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Elemental analysis was performed on a Perkin-Elmer CHNS/O Analyzer 2400II (Perkin-Elmer, Waltham, MA, USA). IR spectra were recorded on a FT/IR 4200 spectrometer (JASCO, Tokyo, Japan) for solid samples (as KBr pellets). NMR spectra were recorded on a ECA-600 spectrometer (JEOL, Tokyo, Japan). Magnetic susceptibilities of the cobalt(II) complexes were determined by the Evans method using the 1H-NMR spectra of the CDCl3 solutions (measured at ambient temperature). UV-vis spectra were measured on a V650 spectrometer (JASCO, Tokyo, Japan). Cyclic voltammetry was performed on a Model 600C Electrochemical Analyzer (ALS, Tokyo, Japan). Gas chromatography (GC) analysis was performed on a GC2010 gas chromatograph (Shimadzu, Kyoto, Japan) equipped with an Rtx-5 column (length = 30 m, i.d. = 0.25 mm, thickness = 0.25 μm, Restek, Bellefonte, PA, USA).
NaToM [14 ] and LPh [16 (link)] were prepared according to the literature. All manipulations were performed under argon by standard Schlenk techniques. THF, toluene, CH2Cl2, and MeCN were purified over a Glass Contour Solvent Dispensing System under Ar atmosphere. meta-Chloroperbenzoic acid (mCPBA) was washed with KH2PO4-NaOH buffer solution (pH 7.4) and pure water to remove meta-chlorobenzoic acid. Other reagents of the highest grade commercially available were used without further purification.
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