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

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

Nuclear Magnetic Resonance (NMR) is predicated at the indisputable fact that convinced nuclei show a magnetic second, orient by way of a magnetic box, and take in attribute frequencies within the radiofrequency a part of the spectrum. The spectral strains of the nuclei are hugely encouraged through the chemical surroundings i.e. the constitution and interplay of the molecules. NMR is now the top strategy 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 accordingly of significant curiosity to all scientists and engineers who intend to take advantage of NMR to check the constitution and the binding of molecules. quantity III/35 "NMR-Data" is split into numerous subvolumes and components. Subvolume III/35A comprises the nuclei 11Band 31P, subvolume III/35B includes the nuclei 19Fand 15N, subvolume III/35C comprises the nucleus 1H, subvolume III/35D includes the nucleus 13C, and subvolume III/35E comprises the nucleus 17O. extra nuclei might be provided later.

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Additional info for Chemical Shifts and Coupling Constants for Hydrogen-1. Part 2: Heterocycles

Example text

4 Coupling constant No. 0(a;b) 47 Ref. 91Yam 87Boo 81Ahl 89Yam2 91Dub 88Nor 96Bry 89Nij 70Arm 96Gme 77Bar 83Tam 92Ade 83Bie 98Kit 92Bro 88Dal 89Yos 99Abe 84Aki 83Kae 78Mat 95Yam 99Abe 84Lai 70Wak 75Sel 70Wak 89Gri 80Mah 70Dic2 99Sez 99Zha 85Aki 79Dri 80Ash 92Min1 99Sel 74Mah 74Beg 2 Hydrogen−1 NMR 48 No. 0(c,2H;e,2H) Ref. 4 Coupling constant No. 0(a,3H;e,2H) 49 Ref. 74Omo 74Wak1 80Bai 95Pur 81Hew 75Coo 82Dan 84Chi 90Eji 82Hol1 88Bur 80Smi 98Mar 74Nas 80Nad 85Bos 75Wor 73Jon 99Erb 80Tew 83Oha 84Seb 99Att 90Lee2 92Dav 90Kas2 85Hei 83Nik 97Att 89Yan 81Jer 78Gel 95Rut 95Per 82Goo 79Gia 91Tra 80Smi 96Mol2 85Moy 70Goo 2 Hydrogen−1 NMR 50 No.

0(a,3H;d,2H) Landolt−Börnstein New Series III/35C,Part−2 37-1 Ref. 4 Coupling constant No. 0(c) 37-2 Ref. 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.

4 Coupling constant No. 0(a,3H;d,2H) Landolt−Börnstein New Series III/35C,Part−2 37-1 Ref. 4 Coupling constant No. 0(c) 37-2 Ref. 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.

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