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5 protocols using nexus 870 ftir spectrometer

1

Spectroscopic Analysis of Dehydroabietic Acid

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IR spectra were measured on a Nexus 870 FTIR spectrometer (Thermo Fisher Scientific, Waltham, MA, USA), and the absorption bands are expressed in cm−1. The HRMS spectra were recorded on a high-resolution mass spectrometer equipped with electrospray (ESI) and nanospray sources, and a quadrupole-time of flight hybrid analyzer (Q-TOF Premier/nanoAquity, Waters, Milford, MA). 1H NMR and 13 C NMR spectra were accomplished in CDCl3 on a Bruker AV-300, AV-500 and DRX-600 NMR spectrometer (Billerica, MA, USA) using TMS as internal standard. Reactions and the resulted products were monitored by TLC which was carried out on TLC Silica gel 60 F254 Aluminium sheets from Merck KGaA, Darmstadt, Germany and visualised in UV light (254 nm). Silica gel (3 0 0–400 mesh) for column chromatography was purchased from Qingdao Marine Chemical Factory, China. The reagents (chemicals), all being of A.R. grade, were purchased from Shanghai Chemical Reagent Company (Shanghai, China) and Energy Chemical (Shanghai, China). Disproportionated rosin was provided by Zhongbang Chemicals Co., Ltd. (Zhaoqing, China), from which dehydroabietic acid (97%) was isolated according to the published method38 .
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2

Synthesis and Characterization of Compounds

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Melting points were measured on an XT-4 apparatus (Taike Corp., Beijing, China) and were uncorrected. IR spetra were measured on a Nexus 870 FT-IR spectrometer (Thermo Fisher Scientific, Waltham, MA, USA), and the absorption bands were expressed in cm−1. The HRMS spectra were recorded on a high-resolution mass spectrometer equipped with electrospray (ESI) and nanospray sources, and a quadrupole-time of flight hybrid analyzer (Q-TOF Premier/nanoAquity, Waters, Milford, MA, USA). 1H and 13C NMR spectra were obtained in CDCl3 on a Bruker DRX-600 NMR spectrometer (Billerica, MA, USA) using TMS as internal standard. Reactions and the resulted products were monitored by TLC which was carried out on TLC Silica gel 60 F254 Aluminum sheets from Merck KGaA, Darmstadt, Germany, and visualized in UV light (254 nm). Silica gel (300–400 mesh) for column chromatography was purchased from Qingdao Marine Chemical Factory (Qingdao, China). The reagents (chemicals), all being of A.R. grade, were purchased from Shanghai Chemical Reagent Company (Shanghai, China) and Energy Chemical (Shanghai, China). Ursolic acid (95%) was bought from Jingzhu Biological Technology Co., Ltd. (Nanjing, China).
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3

Characterization of Organic Compounds

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Melting points were measured on an XT-4 apparatus (Taike Corp., Beijing, China) and were uncorrected. IR spectra were measured on a Nexus 870 FT-IR spectrometer (Thermo Fisher Scientific, Waltham, MA, USA), and the absorption bands were expressed in cm−1. The HRMS spectra were recorded on a high-resolution mass spectrometer equipped with electrospray (ESI) and nanospray sources, and a quadrupole time of flight hybrid analyser (Q-TOF Premier/nanoAquity, Waters, Milford, MA, USA). 1H and 13 C NMR spectra were obtained in CDCl3 on Bruker AV-300, AV-500 (Billerica, MA, USA) and DRX-600 NMR spectrometers using TMS as internal standard. Reactions and the resulted products were monitored by TLC which was carried out on TLC Silica gel 60 F254 Aluminium sheets from Merck KGaA, Darmstadt, Germany and visualised in UV light (254 nm). Silica gel (300 ∼ 400 mesh) for column chromatography was purchased from Qingdao Marine Chemical Factory, China. The reagents (chemicals), all being of A.R. grade, were purchased from Shanghai Chemical Reagent Company (Shanghai, China) and Energy Chemical (Shanghai, China). UA (95%) was bought from Jingzhu Biological Technology Co., Ltd. (Nanjing, China).
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4

Flavonoid Analysis of Citrus limetta

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Citrus limetta was collected from local gardens. Rutin with HPLC grade, methanol, nitric acid, and acetic acid was purchased from Sigma‐Aldrich Inc., and graphene oxide nanoplatelets (99%, Thickness 3.4–7 nm with 6–10 Layers) were used as received. Fourier transform infrared spectroscopy (FTIR) was recorded using KBr tablets on a Thermo Nicolet Nexus 870 FTIR spectrometer. Scanning electron microscope (SEM) was taken using an MIRA3\\TESCAN‐XMU model. The samples were studied by thermogravimetric analysis (TGA) (Netzsch TG 209 F1 Iris1) under nitrogen gas atmosphere (10℃/min). The concentration of flavonoids was measured by variable‐wavelength UV‐Vis spectrophotometry of Unico UV 2100 Model. High‐performance liquid chromatography (HPLC) was performed with an Agilent Technologies 1200 liquid chromatograph which equipped to a quaternary solvent‐delivery system (an auto sampler and a UV detector). An Agilent Zorbax SB‐C18 column (100 × 4.6 mm, 5 μm particle size) was used for all analyses. An ultrasonic bath with temperature control (Elmasonic, S60H) was used to disperse the GO in solution.
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5

Infrared Spectroscopy of PANI Films

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A Thermo Nicolet NEXUS 870 FTIR Spectrometer (Madison, WI 537 11, USA) in a dry air purged environment with a DTGS TEC (deuterated triglycine sulfate thermoelectric cooled) detector in the wavelength range 400 to 4000 cm -1 was used to measure infrared spectra.
Measurements of PANI-CH and PANI-SH dispersions deposited on silicon supports were performed ex situ in transmission mode. Optical micrographs of the studied films deposited on a silicon window were captured using research grade Leica DM LM microscope with objective magnification 50x.
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