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    Vi Viia Viib Viic Viii Ixa Ixb Ixc Ixd Ixe Ixf Ixg X

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    Petcu Ileana
    The document describes 10 dyes (VI-X), reporting their molecular formulas, masses, UV-VIS absorption spectra, elemental analyses, and functional groups identified by infrared spectroscopy. Key details reported include the dyes' λmax values in the range of 340-660 nm, elemental analyses matching calculated compositions, and identification of functional groups including -N=N-, >C=N-, -C-OH, -CONHR, and CH3 groups.

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    Vi Viia Viib Viic Viii Ixa Ixb Ixc Ixd Ixe Ixf Ixg X

    Uploaded by

    Petcu Ileana
    32 views3 pages
    The document describes 10 dyes (VI-X), reporting their molecular formulas, masses, UV-VIS absorption spectra, elemental analyses, and functional groups identified by infrared spectroscopy. Key details reported include the dyes' λmax values in the range of 340-660 nm, elemental analyses matching calculated compositions, and identification of functional groups including -N=N-, >C=N-, -C-OH, -CONHR, and CH3 groups.

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    Dye

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    The document describes 10 dyes (VI-X), reporting their molecular formulas, masses, UV-VIS absorption spectra, elemental analyses, and functional groups identified by infrared spectroscopy. Key details reported include the dyes' λmax values in the range of 340-660 nm, elemental analyses matching calculated compositions, and identification of functional groups including -N=N-, >C=N-, -C-OH, -CONHR, and CH3 groups.

    Copyright:

    Attribution Non-Commercial (BY-NC)
    Download as DOC, PDF, TXT or read online from Scribd
    Download as doc, pdf, or txt
    32 views3 pages

    Vi Viia Viib Viic Viii Ixa Ixb Ixc Ixd Ixe Ixf Ixg X

    Uploaded by

    Petcu Ileana
    The document describes 10 dyes (VI-X), reporting their molecular formulas, masses, UV-VIS absorption spectra, elemental analyses, and functional groups identified by infrared spectroscopy. Key details reported include the dyes' λmax values in the range of 340-660 nm, elemental analyses matching calculated compositions, and identification of functional groups including -N=N-, >C=N-, -C-OH, -CONHR, and CH3 groups.

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    Dye Molecular formula Masa UV – VIS Spectra(DMF) Concentration

    (Kg/mol)
     max (nm log  mol/l
    )
    VI 239 465 1.99
    VIIa 358 436 2.89
    VIIb 372 500 4.86
    VIIc 436.5 530 1.48
    VIII 408 513 0.36
    IXa 223 480 4.85
    IXb 268 425/490 4.89/0.22
    IXc 271.5 340/450 4.86/4.72
    IXd 360 374/480 0.90/1.5
    IXe 253 338/660 0.80/3.09
    IXf 267 345/530 4.83/3.75
    IXg 317.5 350/490 4.80/4.86
    X 504 390/500 3.65/4.87

    Dye Elemental analysis


    C calc
    /C found H calc
    /H found N calc
    /N found
    VI 60.25/60.29 3.77/3.79 29.20/20.26
    VIIa 63.69/63.66 3.91/3.92 23.46/23.48
    VIIb 64.51/64.54 4.30/4.27 22.58/22.60
    VIIc 57.73/57.77 3.89/3.90 20.59/20.60
    VIII 67.64/67.63 3.92/3.90 20.59/20.60
    IXa 64.57/64.53 4.04/4.01 31.39/31.35
    IXb 53.73/53.70 2.99/3.02 31.34/31.33
    IXc 57.47/57.47 3.68/3.65 25.78/25.79
    IXd 50.00/50.02 4.44/4.41 23.33/23.32
    IXe 61.66/61.63 4.34/4.31 27.66/27.62
    IXf 61.66/61.63 3.37/3.39 26.22/26.20
    IXg 52.91/52.89 3.78/3.75 22.05/22.02
    X 61.90/61.87 3.97/3.99 27.78/27.75
    Dye Functional group Frequency (cm -1)
    VI -N = N- 1570 v weak
    >C = N- V c = N 1670 m
    -C – OH(phenol) 1210 i
    VIIa -N = N- 1570 v weak
    >C = N- V c = N 1670 m
     C OH (phenol) 1210 i
    - CONHR  CO amide band I 1653 vi
    Secundary amides  NH and  C  N amide band II 1545 I
     CN and  NH amide band III 1305 m.
    Aromatic ring 1,2,4,5 tetra substituted 880m

    VIIb -N = N- 1570 v weak


    >C = N- V c = N 1670 m
     C OH (phenol) 1210 i
    - CONHR  CO amide band I 1653 vi
    Secundary amides  NH and  C  N amide band II 1545 I
     CN and  NH amide band III 1305 m.
    Aromatic ring 1,2,4,5 tetra substituted 880m
     CH 3 as 2960 i
    2870 m
     CH 3 sim

    VIIc -N = N- 1570 v weak


    >C = N- V c = N 1670 m
     C OH (phenol) 1210 i
    - CONHR  CO amide band I 1653 vi
    Secundary amides  NH and  C  N amide band II 1545 I
     CN and  NH amide band III 1305 m.
    Aromatic ring 1,2,4,5 tetra substituted 880 m
    CH 3 O- 2840 m
    VIII -N = N- 1570 v weak
    >C = N- V c = N 1653 m
     C OH (phenol) 1210 i
    - CONHR  CO amide band I 1653 vi
    Secundary amides  NH and  C  N amide band II 1545 I
     CN and  NH amide band III 1305 m.

    IXa -N = N- 1570 v weak


    IXb -N = N- 1570 v weak
    1517
    -NO 2
    IXc -N = N- 1570 v weak
     CH 3 as 2960 i
     CH 3 sim 2870 m
    -Cl aroma 780

    IXd -N = N- 1570 v weak


    CH 3 O- 2840 m
    RSO 2 -N< SO 2 as 1350 vi
    SO 2 sim 1175 vi
    IXe -N = N- 1570 v weak
    CH 3 O- 2840 m

    IXf -N = N- 1570 v weak


     C Oorg .acid 1710 m

    IXg -N = N- 1570 v weak


    CH 3 O- 2840 m
    -Cl aroma 780

    X -N = N- 1570 v weak
    CH 3 O- 2840 m

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