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Av400

Manufactured by Agilent Technologies

The AV400 is a high-performance nuclear magnetic resonance (NMR) spectrometer manufactured by Agilent Technologies. It is designed to provide accurate and reliable analysis of chemical samples. The core function of the AV400 is to generate and detect radio frequency signals for the purpose of NMR spectroscopy.

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2 protocols using av400

1

Cobalt-Porphyrin Catalyzed Alkyne Functionalization

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All manipulations were performed under a nitrogen atmosphere using standard Schlenk techniques. All solvents used for catalysis were dried over and distilled from sodium (toluene) or CaH2 (dichloromethane, hexane, ethyl acetate, methanol). All the cobalt-porphyrin catalysts [CoII(P1)], [CoII(P2)] [CoII(P3)], and N tosylhydrazone sodium salts were synthesized according to published procedures.7a (link),8 (link),11 (link) All the alkynes were used as purchased from Aldrich. All other chemicals were purchased from commercial suppliers and used without further purification. NMR spectra (1H and 13C) were measured on a Varian INOVA 500 MHz (125 MHZ for 13C), a Bruker AV400 (100 MHZ for 13C) or a Varian MERCURY 300 MHz (75 MHZ for 13C) spectrometer. Mass spectra of the newly synthesised compounds were recorded in Agilent-5973 GC-MS spectrometer the corresponding HRMS data were recorded on JEOL AccuTOF 4G via direct injection probe. Elemental analysis of the newly synthesized complexes were performed by the Mikroanalytisches Laboratorium Kolbe, Germany. EPR spectra were recorded on a Bruker EMXplus spectrometer.
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2

Synthesis of (Diphenylphosphanyl)methyl-6-methyl-pyridine

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All reactions and manipulations were carried out under an atmosphere of dry dinitrogen by using standard Schlenk techniques or in a glovebox. All solvents were purged with dinitrogen and dried with an MBraun Solvent Purification System (SPS); 1H, 13C, 31P, 29Si NMR spectra were recorded with a Bruker AV 300, Bruker DRX 300, Bruker AV 400, or Varian Mercury 300 spectrometer at room temperature unless noted otherwise. Chemical shifts were expressed relative to residual 1H, 13C solvent signals, 85 % H3PO4, and external tetramethylsilane, respectively. Mass spectra were recorded with an AccuTOF LC, JMS‐T100LP, AccuTOF GC v 4g, or JMS‐T100GCV mass spectrometer. IR spectra were recorded with a Bruker Vertex 70v spectrometer. Elemental analyses were carried out by Kolbe Mikroanalytisches Labor, Oberhausen (Germany). (Diphenylphosphanyl)methyl‐6‐methyl‐pyridine was prepared according to a literature procedure.29
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