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Iraffinity 1 ftir

Manufactured by Shimadzu
Sourced in United States, Japan

The IRAffinity-1 FTIR is a Fourier Transform Infrared Spectrometer designed for routine analysis. It features a high-performance optical system and advanced software to provide accurate and reliable infrared spectroscopy data.

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6 protocols using iraffinity 1 ftir

1

Comprehensive Spectroscopic Characterization of Synthesized Compounds

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All reagents were used without any further purification. Melting points were observed using Electrothermal Melting Point apparatus, LABCO Co., India and are not corrected. The FT-IR spectra were recorded in KBr on IR affinity-1 FTIR (Shimadzu) spectrophotometer, and results are reported in cm−1. 1H NMR and 13C NMR spectra were recorded on Bruker AVANCE III NMR spectrometer operating at 400 and 100 MHz, respectively, with CDCl3 as the solvent and tetramethylsilane (TMS) as the internal standard. Chemical shifts (δ) are reported in parts per million (ppm), and coupling constants (J) are expressed in Hertz (Hz). HRMS were obtained from Waters Synapt G2-Si QTOF and SCIEX 5600+ QTOF mass analyser by using the electrospray ionization (ESI) method. The purity of synthesized compounds was checked by precoated TLC plates (SIL G/UV254, ALUGRAM) using a mixture of hexane and ethyl acetate as eluent and visualization was achieved via UV light.
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2

Characterization of Magnetic Nanoparticles by FTIR

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Fourier transform infrared spectroscopy (FTIR) spectra of approximately 2 mg of dried MNPs were recorded using an IRAffinity-1 FTIR (Shimadzu Scientific Instruments, KS, USA). For each spectrum, 45 scans were collected between 4000 and 400 cm−1 at a resolution of 1 cm−1.
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3

Spectroscopic Characterization of Natural Products

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Optical rotations were measured on a Jasco DIP-370 Digital Polarimeter at the sodium line (589 nm). UV absorbances were measured on a Varian Cary 50 Bio UV-Vis Spectrophotometer. IR spectroscopy was measured as a thin film on a CaF2 disk using a Shimadzu IRAffinity-1 FTIR. 1H, 13C NMR and 2D NMR experiments on the natural products were carried out on Varian Unity Inova 500 MHz spectrometer. NMR spectra were referenced to the appropriate residual solvent signal (δH 7.26, δC 77.0 for CDCl3). The HSQC experiments were optimized for 1JC,H = 140 Hz and HMBC experiments for 3JC,H = 7 Hz. High-resolution mass spectrometric data were obtained on a Agilent 6210 TOF LC/MS using the ESI source in positive mode.
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4

Synthesis and Characterization of Spirothiazolidinones

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Chemicals were obtained from Sigma Aldrich. Reaction progress was monitored by thin layer chromatography (TLC) using silica gel plates and chloroform:methanol (9:1) as the eluent. Melting points (mp) were determined on a Buchi B-540 capillary melting point apparatus in open capillaries and uncorrected. IR spectra were recorded in KBr discs on a Shimadzu IR Affinity-1 FTIR. 1 H NMR (DMSO-d 6 ) spectra were run on a
Varian MERCURY 400 MHZ and 13 C NMR (APT) (DMSO-d 6 ) spectra were run Bruker 500 MHz spectrophotometers. Microanalyses were performed on a Thermo Finnigan Flash EA 1112 elemental analyzer.
(Sp: spirothiazolidinone, Ar: aromatic ring).
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5

Exploring Drug-Vesicle Interactions via FT-IR

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An IR spectrophotometer equipped with Shimadzu IR Affinity-1 FT-IR (Shimadzu, Japan) was used to study the interaction between the drug and the ENV system to determine the influence of the vesicle membrane component on the drug. When a drug interacts with the compounds in the NV system, the IR spectrum of the physical mixture corresponding to the drug exhibits additional peaks or does not contain characteristic peaks (Ţucureanu et al. 2016) . The FT-IR peaks from 400 cm -1 to 4000 cm -1 were assessed to find any additional or missing peaks from the fingerprint and the functional region (Arkin 2013).
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6

Characterization of Inorganic Compounds

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Unless otherwise specified, all reagents and starting materials were of reagent grade or better and purchased from standard suppliers and used as received. Water was purified by reverse osmosis. Where anhydrous solvents were required, HPLCgrade solvent was either distilled from standard drying agents or dried by passing over a sealed column of activated alumina.
Powder X-ray diffraction patterns were obtained using a GBC-MMA diffractometer operating at 1.0 kW with samples mounted on 1" quartz substrates. Simultaneous thermogravimetric-differential thermal analysis (TG-DTA) traces were obtained using a Shimadzu DTG-60 instrument fitted with a FC-60A flow rate controller and TA-60WS thermal analyser using measuring parameters of 10 °C per min under nitrogen flow of 20 cm 3 min -1 . Infrared spectra were obtained using a Shimadzu IR Affinity-1 FTIR, fitted with a MIRacle 10 single reflection ATR accessory. Microanalyses were recorded by Mr Alan Carver (University of Bath Microanalysis Service) or Gillian Maxwell (University College London Microanalysis Service) or the Microanalytical Unit, Australian National University, Australia or the Campbell Microanalytical Laboratory, University of Otago, New Zealand.
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