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diode-array uv–vis–nir spectrometer avantes avaspec  (Avantes Inc)

 
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    Structured Review

    Avantes Inc diode-array uv–vis–nir spectrometer avantes avaspec
    Diode Array Uv–Vis–Nir Spectrometer Avantes Avaspec, supplied by Avantes Inc, used in various techniques. Bioz Stars score: 90/100, based on 1 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/diode+array+uv-vis-nir+system/diode+array+uv+vis+nir+spectrometer+avantes+avaspec/pmc09967363-237-9-12
    Average 90 stars, based on 1 article reviews
    diode-array uv–vis–nir spectrometer avantes avaspec - by Bioz Stars, 2026-09
    90/100 stars

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    Related Articles

    other:

    Article Title: Synthesis, structure and redox chemistry of the aminoallenylidene complex [Mo{C C C(Me)NEt2}(dppe)(η-C7H7)][BPh4]
    Article Snippet: Spectra were recorded on an Agilent Technologies Cary 660 FTIR or an Avantes diode array UV-Vis-NIR system comprising two light sources (UV-Vis: AvaLight-DH-S-Bal, Vis-NIR: AvaLightHal-S) and two spectrometers (UV-Vis: AvaSpec-ULS204-8L-USB2, NIR: AvaSpec-NIR256-2.5TEC) connected to a custom-built sample holder by bifurcated fibre optic cables.

    Article Title: A Spectroscopic and Computationally Minimal Approach to the Analysis of Charge-Transfer Processes in Conformationally Fluxional Mixed-Valence and Heterobimetallic Complexes.
    Article Snippet: Spectra were recorded on an Agilent Technologies Cary 660 FTIR, Agilent Technologies Cary 5000 UV- Vis-NIR or an Avantes diode array UV-Vis-NIR system comprising two light sources (UV-Vis: AvaLight-DH-S-Bal, Vis-NIR: AvaLight-Hal-S) and two spectrometers (UV-Vis: AvaSpec- ULS204-8L-USB2, NIR: AvaSpec-NIR256-2.5TEC) connected to a custom-built sample holder by bifurcated fibre optic cables.



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    (a) <t>UV–vis</t> spectra for the copper(II)– H 2 L 4 (1:1) system with an increasing concentration of EDTA. (b) Measured (filled circle) and fitted (dashed line) absorbances at 420 nm plotted against the EDTA-to-ligand ratio ( c L = 25 μM, c Cu = 25 μM, c EDTA = 0–62.5 μM, 30% (v/v) DMSO/H 2 O; pH = 5.90, I = 0.1 M (KCl), t = 25 °C).
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    (a) <t>UV–vis</t> spectra for the copper(II)– H 2 L 4 (1:1) system with an increasing concentration of EDTA. (b) Measured (filled circle) and fitted (dashed line) absorbances at 420 nm plotted against the EDTA-to-ligand ratio ( c L = 25 μM, c Cu = 25 μM, c EDTA = 0–62.5 μM, 30% (v/v) DMSO/H 2 O; pH = 5.90, I = 0.1 M (KCl), t = 25 °C).
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    (a) <t>UV–vis</t> spectra for the copper(II)– H 2 L 4 (1:1) system with an increasing concentration of EDTA. (b) Measured (filled circle) and fitted (dashed line) absorbances at 420 nm plotted against the EDTA-to-ligand ratio ( c L = 25 μM, c Cu = 25 μM, c EDTA = 0–62.5 μM, 30% (v/v) DMSO/H 2 O; pH = 5.90, I = 0.1 M (KCl), t = 25 °C).
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    Image Search Results


    (a) UV–vis spectra for the copper(II)– H 2 L 4 (1:1) system with an increasing concentration of EDTA. (b) Measured (filled circle) and fitted (dashed line) absorbances at 420 nm plotted against the EDTA-to-ligand ratio ( c L = 25 μM, c Cu = 25 μM, c EDTA = 0–62.5 μM, 30% (v/v) DMSO/H 2 O; pH = 5.90, I = 0.1 M (KCl), t = 25 °C).

    Journal: Journal of Medicinal Chemistry

    Article Title: Copper(II) Complexes with Isomeric Morpholine-Substituted 2-Formylpyridine Thiosemicarbazone Hybrids as Potential Anticancer Drugs Inhibiting Both Ribonucleotide Reductase and Tubulin Polymerization: The Morpholine Position Matters

    doi: 10.1021/acs.jmedchem.4c00259

    Figure Lengend Snippet: (a) UV–vis spectra for the copper(II)– H 2 L 4 (1:1) system with an increasing concentration of EDTA. (b) Measured (filled circle) and fitted (dashed line) absorbances at 420 nm plotted against the EDTA-to-ligand ratio ( c L = 25 μM, c Cu = 25 μM, c EDTA = 0–62.5 μM, 30% (v/v) DMSO/H 2 O; pH = 5.90, I = 0.1 M (KCl), t = 25 °C).

    Article Snippet: The cell was positioned in the CUV-UV Cuvette Holder (Ocean Optics) connected to the diode array UV–vis-NIR spectrometer by optical fibers.

    Techniques: Concentration Assay

    (a) Time-dependent UV–vis absorption spectra of complex 6 (copper(II)– H 2 L 6 (1:1) system) in the presence of GSH (50 equiv) before (red line) and after mixing the solutions (black/gray lines) in a tandem cuvette under anoxic conditions. The absorbance changes after bubbling oxygen into the reaction mixture (blue line). (b) Plot of the time-dependent absorbance changes at 406 nm for 6 (cross, black line), at 396 nm for 4 (square, green line), at 398 nm for 5 (circle, red line), and at 398 nm for 3 (triangle, blue line) (50 mM HEPES, pH = 7.4); solvent: water; c Cu = c L = 25 μM; c GSH = 1.25 mM; I = 0.1 M (KCl); t = 25 °C).

    Journal: Journal of Medicinal Chemistry

    Article Title: Copper(II) Complexes with Isomeric Morpholine-Substituted 2-Formylpyridine Thiosemicarbazone Hybrids as Potential Anticancer Drugs Inhibiting Both Ribonucleotide Reductase and Tubulin Polymerization: The Morpholine Position Matters

    doi: 10.1021/acs.jmedchem.4c00259

    Figure Lengend Snippet: (a) Time-dependent UV–vis absorption spectra of complex 6 (copper(II)– H 2 L 6 (1:1) system) in the presence of GSH (50 equiv) before (red line) and after mixing the solutions (black/gray lines) in a tandem cuvette under anoxic conditions. The absorbance changes after bubbling oxygen into the reaction mixture (blue line). (b) Plot of the time-dependent absorbance changes at 406 nm for 6 (cross, black line), at 396 nm for 4 (square, green line), at 398 nm for 5 (circle, red line), and at 398 nm for 3 (triangle, blue line) (50 mM HEPES, pH = 7.4); solvent: water; c Cu = c L = 25 μM; c GSH = 1.25 mM; I = 0.1 M (KCl); t = 25 °C).

    Article Snippet: The cell was positioned in the CUV-UV Cuvette Holder (Ocean Optics) connected to the diode array UV–vis-NIR spectrometer by optical fibers.

    Techniques: Solvent

    (a) CVs of 6 (black trace—first scan, red trace—second scan) in DMSO/ n -Bu 4 NPF 6 at the Pt working electrode at a scan rate of 100 mV s –1 . (b) UV–vis spectra measured upon cathodic reduction of 6 at the first reduction peak by using a honeycomb Pt working electrode (inset: (black trace) EPR spectrum of 6 in DMSO; (red and blue trace) EPR spectra of 6 in DMSO after cathodic reduction at the first cathodic peak.)

    Journal: Journal of Medicinal Chemistry

    Article Title: Copper(II) Complexes with Isomeric Morpholine-Substituted 2-Formylpyridine Thiosemicarbazone Hybrids as Potential Anticancer Drugs Inhibiting Both Ribonucleotide Reductase and Tubulin Polymerization: The Morpholine Position Matters

    doi: 10.1021/acs.jmedchem.4c00259

    Figure Lengend Snippet: (a) CVs of 6 (black trace—first scan, red trace—second scan) in DMSO/ n -Bu 4 NPF 6 at the Pt working electrode at a scan rate of 100 mV s –1 . (b) UV–vis spectra measured upon cathodic reduction of 6 at the first reduction peak by using a honeycomb Pt working electrode (inset: (black trace) EPR spectrum of 6 in DMSO; (red and blue trace) EPR spectra of 6 in DMSO after cathodic reduction at the first cathodic peak.)

    Article Snippet: The cell was positioned in the CUV-UV Cuvette Holder (Ocean Optics) connected to the diode array UV–vis-NIR spectrometer by optical fibers.

    Techniques: