Ft ir 4600 ft ir spectrometer

Manufactured by Jasco

The FT/IR-4600 FT-IR Spectrometer is a Fourier Transform Infrared (FT-IR) spectroscopy instrument. It is designed to analyze the infrared absorption and emission characteristics of various materials. The device utilizes an interferometer to generate and detect infrared radiation, providing information about the molecular composition and structure of the sample under analysis.

Automatically generated - may contain errors

Lab products found in correlation

Vnmrs 600, by Agilent Technologies (1 mentions) Vnmrs 500, by Agilent Technologies (1 mentions) Autoflex speed maldi mass spectrometer, by Bruker (1 mentions) Mercury 400, by Agilent Technologies (1 mentions) Spectra manager version 2, by Jasco (1 mentions) Cobalt 2 acetate, by Merck Group (1 mentions) Pw1730, by Philips (1 mentions) Cellulose nanofibers, by Merck Group (1 mentions) Vista pro ccd simultaneous icp oes instrument, by Agilent Technologies (1 mentions) Iron 2 sulfate, by Merck Group (1 mentions) Em208 microscope, by Philips (1 mentions) Sodium hydroxide (naoh), by Merck Group (1 mentions) Iron 3 chloride, by Merck Group (1 mentions) Mira3, by TESCAN (1 mentions)

Spelling variants of this product

FT/IR-4600 (62 citations) FT/IR-4600 spectrometer (40 citations) FT/IR-4600 Fourier transform infrared spectrometer (6 citations) 4600 spectrometer (3 citations) FT/IR-4600 typeA spectrometer (2 citations)

4 protocols using ft ir 4600 ft ir spectrometer

Iridium-Catalyzed C-H Sulfonation of Heterocycles

Check if the same lab product or an alternative is used in the 5 most similar protocols

All synthetic procedures were performed under nitrogen either in a Vacuum Atmospheres glovebox or in a closed reactor. Acetophenone, 4-toluenesulfonyl chloride, 4-fluorobenzenesulfonyl chloride, 2-picolylamine, [Cp*IrCl₂]₂, potassium tert-butoxide, formic acid (97%), and NaHCO₃ were purchased from common vendors and used without further purification. NMR solvents (CD₂Cl₂, CDCl₃, and C₆D₆), 2-propanol, and triethylamine were dried and distilled over CaH₂. Hexane and CH₂Cl₂ were dried using a solvent purification system.
¹H, ¹³C, and ¹⁹F NMR spectra were acquired on Varian Mercury 400, VNMRS-500, and VNMRS-600 spectrometers and processed using MestReNova 12.0.1. All chemical shifts are reported in ppm and referenced to the residual ¹H or ¹³C solvent peaks. Following abbreviations are used: (s) singlet, (bs s) broad singlet, (d) doublet, (t) triplet, (dd) doublet of doublets, etc. NMR spectra of all metal complexes were taken in 8” J. Young tubes (Wilmad or Norell) with Teflon valve plugs. MALDI-MS spectra were acquired on Bruker Autoflex Speed MALDI Mass Spectrometer. X-ray crystallography data were obtained on a Bruker APEX DUO single-crystal diffractometer equipped with an APEX2 CCD detector, Mo fine-focus and Cu micro-focus X-ray sources. IR spectra were obtained using Jasco FT/IR-4600 FT-IR Spectrometer.

Demianets I., Cherepakhin V., Maertens A., Lauridsen P.J., Sharada S.M, & Williams T.J. (2020). A New Mechanism of Metal-Ligand Cooperative Catalysis in Transfer Hydrogenation of Ketones. Polyhedron, 182, 114508.

+ Open protocol

+ Expand

Micro FT-IR Spectroscopy of Samples

Check if the same lab product or an alternative is used in the 5 most similar protocols

Globar light
micro FT-IR spectroscopy was performed using an IRT-7100 IR microscope
with the FT/IR-4600 FT-IR spectrometer (JASCO) equipped with a high
brilliant ceramic light source, liquid nitrogen-cooled single mid-band
MCT detector, and 32× Cassegrain objective (NA = 0.75). FT-IR
spectra were recorded in transmission mode as the average of 256 scans
from 600 to 4000 cm^–1 at a spectral resolution of
4 cm^–1, with an aperture size of 10 × 10 μm². The measurement points were scanned at 2.5 × 2.5 and
10 × 10 μm², and the spectra were converted
to text data files using Spectra Manager version 2 (JASCO).

Iwai T., Honda S., Watanabe S., Matsushita R., Nakanishi T., Takatsu M., Moriwaki T., Yabashi M., Ishikawa T, & Seto Y. (2023). Forensic Discrimination of Drug Powder Based on Drug Mixing Condition Determined Using Micro Fourier Transform Infrared Spectroscopy. ACS Omega, 8(4), 4285-4293.

+ Open protocol

+ Expand

Characterization of Organometallic Complexes

Check if the same lab product or an alternative is used in the 5 most similar protocols

All of the materials for synthesis were purchased from commercial suppliers and used without further purification. The absorption spectra were recorded on a Shimadzu UV-PC-2401 UV-vis spectrophotometer using 10 mm path length quartz cuvettes in the range 300−800 nm wavelengths, while the fluorescence measurements were carried on a Horiba Jobin-Yvon FluoroMax-4 spectrofluorometer using 10 mm path length quartz cuvettes with a slit width of 5 nm at 298 K. FT–IR spectra were measured on a JASCO FTIR 4600 FT–IR spectrometer with 4 cm⁻¹ resolution and 32 scanned between wave number 4000 cm⁻¹ and 400 cm⁻¹. Samples were prepared KBr disks with 1 mg of complex in 100 mg of KBr. The mass spectra of RH using Agilent Technologies 6520 Accurate mass spectrometer. NMR spectra were recorded on a Varian FT-400 MHz instrument. The chemical shifts were recorded in parts per million (ppm) on the scale. The following abbreviations are used to describe spin multiplicities in ¹H NMR spectra: s = singlet; d = doublet; t = triplet; m = multiplet.

Munisamy M., Rathinam B., Shanmugasundaram E., Ganesan V., Narayanan V., Balakrishnan S.B., Kaliyamoorthy S, & Thambusamy S. (2023). β-Cyclodextrin-Encapsulated Rhodamine Derivatives Core–Shell Microspheres—Based Fluorescent Sensor for Au3+ and Template for Generating Microplates of Gold. Micromachines, 14(7), 1443.

+ Open protocol

+ Expand

Synthesis and Characterization of Magnetic Nanoparticles

Check if the same lab product or an alternative is used in the 5 most similar protocols

Cellulose nanofibers were purchased from Sigma Aldrich. Iron(iii) chloride, iron(ii) sulfate, cobalt(ii) acetate, and sodium hydroxide were purchased from Sigma Aldrich. All chemicals were used without further purification. The FT-IR spectra were recorded on a JASCO FT/IR 4600 FT-IR spectrometer. The thermal analysis (TGA) was carried out using a TGA Q600 TA instrument at a heating rate of 10 °C min⁻¹ in air. The powder X-ray diffraction (XRD) was performed with a Philips PW1730. The scanning electron microscopy (FESEM) and the energy dispersive X-ray spectroscopy (EDS) characterization of catalysts was performed using an electron microscope Tescan MIRA3. The melting points of the products were measured by an electrothermal 9100 apparatus. ICP experiments were accomplished using a Varian Vista Pro CCD simultaneous ICP-OES instrument. Magnetic properties of the nanoparticles were measured with a vibrating sample magnetometer (VSM). Transmission electron microscopy (TEM) was performed on a Philips EM208 microscope and was operated at 100 kV.

Kargar P.G., Bagherzade G, & Eshghi H. (2020). Novel biocompatible core/shell Fe3O4@NFC@Co(ii) as a new catalyst in a multicomponent reaction: an efficient and sustainable methodology and novel reusable material for one-pot synthesis of 4H-pyran and pyranopyrazole in aqueous media. RSC Advances, 10(61), 37086-37097.

+ Open protocol

+ Expand

About PubCompare

Our mission is to provide scientists with the largest repository of trustworthy protocols and intelligent analytical tools, thereby offering them extensive information to design robust protocols aimed at minimizing the risk of failures.

We believe that the most crucial aspect is to grant scientists access to a wide range of reliable sources and new useful tools that surpass human capabilities.

However, we trust in allowing scientists to determine how to construct their own protocols based on this information, as they are the experts in their field.

Ready to get started?

Revolutionizing how scientists
search and build protocols!