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argon ion laser  (HORIBA Ltd)


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    HORIBA Ltd argon ion laser
    Argon Ion Laser, supplied by HORIBA Ltd, used in various techniques. Bioz Stars score: 99/100, based on 8559 PubMed citations. ZERO BIAS - scores, article reviews, protocol conditions and more
    https://www.bioz.com/product/argon/LabRAM+HR+Evolution/pm42046544-83-17-24
    Average 99 stars, based on 8559 article reviews
    argon ion laser - by Bioz Stars, 2026-11
    99/100 stars

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    Related Articles

    Raman Spectroscopy:

    Article Title: Spin state modulation on dual Fe center by adjacent Ni sites enabling the boosted activities and ultra-long stability in Zn-air batteries.
    Article Snippet: Breakthrough in developing cost-effective Fe-based catalysts with superior oxygen reduction reaction (ORR) activities and ultra-long-term stability for application in Zn-air batteries (ZABs) remain a priority but still full of challenges.. Herein, the neighboring NiN4 single-metal-atom and Fe2N5 dual-metal-atoms on the N-doped hollow carbon sphere (Fe/Ni-NHCS) were deliberately constructed as the efficient and robust ORR catalyst for ZABs.. Both theory calculations and magnetic measurements demonstrate that the introduction of NiN4 provides a significant role on optimizing the electron spin state of Fe2N5 sites and reducing the energy barrier for the adsorption and conversion of the oxygen-containing intermediates, enabling the Fe/Ni-NHCS with excellent ORR performance and ultralow byproduct HO2 yield (0.5%).



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    Image Search Results


    ( A ) Previously developed sulfonyl‐based solid support strategy for the incorporation of amino modifiers ( S ‐CPG). In some implementations, S ‐CPG can also be conjugated to the solid support through a carbamate linkage. ( B ) This work focuses on the use of CPR II CPG to incorporate amino modifiers via initial activation with N , N ′‐disuccinimidyl carbonate (DSC), generating R ‐CPG. A trifunctional ligand (protected 1,3‐diamino‐2‐propanol) enables anchoring to the solid support, followed by selective conjugation at the amine and subsequent strand elongation from the hydroxyl group.

    Journal: Current Protocols

    Article Title: A Facile Strategy for 3′‐Terminal Functionalization of DNA and RNA via On‐Column Conjugation with Integration into Tandem Oligonucleotide Synthesis

    doi: 10.1002/cpz1.70374

    Figure Lengend Snippet: ( A ) Previously developed sulfonyl‐based solid support strategy for the incorporation of amino modifiers ( S ‐CPG). In some implementations, S ‐CPG can also be conjugated to the solid support through a carbamate linkage. ( B ) This work focuses on the use of CPR II CPG to incorporate amino modifiers via initial activation with N , N ′‐disuccinimidyl carbonate (DSC), generating R ‐CPG. A trifunctional ligand (protected 1,3‐diamino‐2‐propanol) enables anchoring to the solid support, followed by selective conjugation at the amine and subsequent strand elongation from the hydroxyl group.

    Article Snippet: Argon gas 1,3‐Diamino‐2‐propanol (Fisher Scientific, cat. no. AAA1961809) 1,8‐Diazabicyclo[5.4.0]undec‐7‐ene (DBU; Combi‐Blocks, cat. no. QA‐1443) 4‐Methoxytrityl chloride (MMTr‐Cl; Tokyo Chemical Industry, cat. no. M0790) Dichloromethane (DCM; ACS grade, Sigma‐Aldrich, cat. no. 34856) Methanol (MeOH; HPLC grade, Sigma‐Aldrich, cat. no. 34860) Silica gel (60 Å, 230‐400 mesh; Fisher Chemical, S82525) Deuterated DMSO (DMSO‐d 6 ; Sigma‐Aldrich, cat. no. 151874‐10 × 0.75ML) 2,5‐Dioxopyrrolidin‐1‐yl 2‐(prop‐2‐yn‐1‐yloxy)acetate (NHS‐ester propargyl; Combi‐Blocks, cat. no. JP‐4311) 200 mM HEPES buffer, pH 8 4 × 35‐cm (diameter × height) flash chromatography column 300‐MHz nuclear magnetic resonance (NMR) instrument (other instruments may be used)

    Techniques: Activation Assay, Conjugation Assay

    Synthesis of protected 1,3‐diamino‐2‐propanol ( A ) for on‐column coupling and subsequent conjugation using NHS‐ester chemistry, illustrated here with propargyl ( B ).

    Journal: Current Protocols

    Article Title: A Facile Strategy for 3′‐Terminal Functionalization of DNA and RNA via On‐Column Conjugation with Integration into Tandem Oligonucleotide Synthesis

    doi: 10.1002/cpz1.70374

    Figure Lengend Snippet: Synthesis of protected 1,3‐diamino‐2‐propanol ( A ) for on‐column coupling and subsequent conjugation using NHS‐ester chemistry, illustrated here with propargyl ( B ).

    Article Snippet: Argon gas 1,3‐Diamino‐2‐propanol (Fisher Scientific, cat. no. AAA1961809) 1,8‐Diazabicyclo[5.4.0]undec‐7‐ene (DBU; Combi‐Blocks, cat. no. QA‐1443) 4‐Methoxytrityl chloride (MMTr‐Cl; Tokyo Chemical Industry, cat. no. M0790) Dichloromethane (DCM; ACS grade, Sigma‐Aldrich, cat. no. 34856) Methanol (MeOH; HPLC grade, Sigma‐Aldrich, cat. no. 34860) Silica gel (60 Å, 230‐400 mesh; Fisher Chemical, S82525) Deuterated DMSO (DMSO‐d 6 ; Sigma‐Aldrich, cat. no. 151874‐10 × 0.75ML) 2,5‐Dioxopyrrolidin‐1‐yl 2‐(prop‐2‐yn‐1‐yloxy)acetate (NHS‐ester propargyl; Combi‐Blocks, cat. no. JP‐4311) 200 mM HEPES buffer, pH 8 4 × 35‐cm (diameter × height) flash chromatography column 300‐MHz nuclear magnetic resonance (NMR) instrument (other instruments may be used)

    Techniques: Conjugation Assay