Chemical Shifts and Coupling Constants for Hydrogen-1. Part by M. Jain (auth.), R. R. Gupta, M. D. Lechner (eds.)

By M. Jain (auth.), R. R. Gupta, M. D. Lechner (eds.)

Nuclear Magnetic Resonance (NMR) relies at the incontrovertible fact that convinced nuclei express a magnetic second, orient by means of a magnetic box, and take up attribute frequencies within the radiofrequency a part of the spectrum. The spectral traces of the nuclei are hugely stimulated via the chemical atmosphere i.e. the constitution and interplay of the molecules. NMR is now the prime approach and a strong instrument for the research of the constitution and interplay of molecules. the current Landolt-Börnstein quantity III/35 "Nuclear Magnetic Resonance (NMR) information" is for this reason of significant curiosity to all scientists and engineers who intend to exploit NMR to check the constitution and the binding of molecules. quantity III/35 "NMR-Data" is split into a number of subvolumes and components. Subvolume III/35A comprises the nuclei 11Band 31P, subvolume III/35B comprises the nuclei 19Fand 15N, subvolume III/35C comprises the nucleus 1H, subvolume III/35D comprises the nucleus 13C, and subvolume III/35E includes the nucleus 17O. extra nuclei could be offered later.

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Extra resources for Chemical Shifts and Coupling Constants for Hydrogen-1. Part 2: Heterocycles

Example text

82Bro 85Ike 74Nag2 00Kou 82Kar 75Bla 82Fir 83Bél 75Sai 75Hul2 88Kyb 91Nit 77Mar 97Shi 89Teu 92Lev 82Fir 97Alv 84Tho 80Dor 99Eic 73Fos 75Hul2 82Hol1 80Shr 78Atk 70Eng1 78Pad 90Got 2 Hydrogen−1 NMR 38 No. Gross formula Solvent 1571 1572 1573 1574 1575 1576 1577 1578 1579 1581 1582 1583 1584 1585 1587 1588 1589 1590 1591 1592 1593 1594 1595 1596 1597 1598 1599 1600 1602 1603 1604 1605 1606 1607 1609 1610 1613 1614 1615 1616 C13H10N2O2 C13H10N2O2 C13H10N2O2 C13H10N2O2 C13H10N2O2 C13H10N2O3 C13H10N2O4 C13H10N4O2S C13H10N4O3S C13H10OS C13H10OS3 C13H10O4 C13H10O5 C13H10S2 C13H11Br2N C13H11Br2NO2 C13H11ClN2O5 C13H11F5O C13H11N C13H11NO C13H11NOS C13H11NO2 C13H11NO2 C13H11NO3 C13H11NO3 C13H11NO3 C13H11NO4 C13H11NO4 C13H11NO6 C13H11NS C13H11N3 C13H11N3O C13H11N3O C13H11N3O2 C13H11N3O4 C13H11N3O5 C13H12ClNO2S C13H12Cl2N4 C13H12F3NO2 C13H12F3NO3 CDCl3 CDCl3 DMSO−d6 DMSO−d6 CDCl3 CF3COOH CDCl3 CDCl3 DMSO−d6 CDCl3 CDCl3 2 [ H]Chloroform CD3COCD3 CDCl3 CD3OD CDCl3 CDCl3 CDCl3 CDCl3 CDCl3 2 [ H6]DMSO CDCl3 CDCl3 CDCl3 DMSO−d6 CDCl3 DMSO−d6 CDCl3 DMSO−d6 CCl4 CDCl3 CDCl3 DMSO−d6 CDCl3 CDCl3 CDCl3 CDCl3 CDCl3 CDCl3 CDCl3 J [Hz] Ref.

Gross formula Solvent 1662 1663 1664 1665 1666 1667 1668 1669 1670 1672 1673 1674 1675 1676 1677 1678 1679 1680 1681 1682 1683 1684 1685 1686 1687 1688 1689 1690 1691 1692 1693 1694 1695 1696 1698 1699 1700 1701 1702 1703 C13H13NO4 C13H13NO4 C13H13NO4 C13H13NO4 C13H13NO4 C13H13NO4S C13H13NO5 C13H13NS2 C13H13N3 C13H13N3O4 C13H13N5O C13H14ClNO4S C13H14ClN3O3 C13H14Cl3NO C13H14F3NO2 C13H14F3NO7S C13H14N2O C13H14N2O C13H14N2O C13H14N2OS C13H14N2O2 C13H14N2O2 C13H14N2O2 C13H14N2O2 C13H14N2O3 C13H14N2O3 C13H14N2O3S C13H14N2O4 C13H14N2O4 C13H14N2O5 C13H14N2O5 C13H14N2O5S C13H14N4O C13H14N4O C13H14N4O3 C13H14N4O4 C13H14OS C13H14O2 C13H14O2 C13H14O2 DMSO−d6 CDCl3 DMSO−d6 CCl4 CF3COOH CDCl3 CDCl3 CDCl3 CDCl3 CD3OD DMSO−d6 CDCl3+CF3COOH CDCl3 CDCl3 2 [ H6]DMSO CD2Cl2 CDCl3 CDCl3 CDCl3 CDCl3 CDCl3 CDCl3 CDCl3 CDCl3 DMSO−d6 CDCl3 CDCl3 CDCl3 CDCl3 CDCl3 CDCl3 DMSO−d6 CDCl3 DMSO−d6 DMSO−d6 DMSO−d6 CDCl3 CDCl3 CDCl3 CDCl3 J [Hz] Ref.

98Mar 89Nad 96Kep 70Bax 86Shr 75Cam 82Aki 90Shi 75Per 97Dan 80Jeg 80Per2 90Lee2 82Heg 78Gel 80Tew 90Kas1 73Fie2 88Mac 81Bak 78Utl 79Kim 84Aki 92Kob 94Roh 71Hic1 84Ram 80Jeg 73Col 95Bou 78Wat 00Bla 96Hua 90Kas2 80Des 95Yam 97Cop 86Tay 73Fie2 89Rei 72Dol 2 Hydrogen−1 NMR 54 No. 0(a,3H;b,2H) Ref. 4 Coupling constant No. Gross formula Solvent 2381 2382 2383 2384 2385 2388 2389 2390 2391 2392 2393 2394 2395 2396 2397 2398 2399 2401 2402 2403 2404 2405 2407 2408 2409 2410 2411 2413 2414 2415 2416 2417 2418 2419 2420 2421 C17H14N4O2 C17H14OS C17H14O2 C17H14O2S C17H14O3 C17H14O3S C17H14O5 C17H14S C17H15Cl2NO C17H15N C17H15N C17H15NO2 C17H15NO2 C17H15NO2 C17H15NO3S C17H15NO4 C17H15N3O C17H15N3O3 C17H15O2P C17H16BrNOS2 C17H16BrN3OS C17H16ClN3 C17H16N2O C17H16N2O C17H16N2OS C17H16N2O2 C17H16N2O3 C17H16N4O3 C17H16O C17H16O2S C17H16O2S C17H16S2 C17H17NO C17H17NO C17H17NO2 C17H17NO2 2423 2424 2426 2427 C17H17NO2S C17H17NO2S C17H17NO4 C17H17NO4 CDCl3 CDCl3 CDCl3 CS2 CDCl3 CDCl3 CD3COCD3 CDCl3 CDCl3 CCl4 CDCl3 CDCl3 CDCl3 CDCl3 CDCl3 CDCl3 DMSO−d6 CDCl3 − CDCl3 Pyridine−d5 CDCl3 DMSO−d6 CDCl3 DMSO−d6 CF3COOD CDCl3 2 [ H6]Acetone CCl4 CS2 CDCl3 CDCl3 CDCl3 CDCl3 CDCl3 CDCl3 31ºC CDCl3 CDCl3 CCl4 CDCl3 Landolt−Börnstein New Series III/35C,Part−2 J [Hz] 55 Ref.

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