15N NMR spectroscopy unambiguously establishes the coordination mode of the diimine linker 2-(2′-pyridyl)pyrimidine-4-carboxylic acid (cppH) in Ru(ii) complexes

2015 ◽  
Vol 44 (35) ◽  
pp. 15671-15682 ◽  
Author(s):  
Federica Battistin ◽  
Gabriele Balducci ◽  
Nicola Demitri ◽  
Elisabetta Iengo ◽  
Barbara Milani ◽  
...  

The 15N NMR chemical shifts, obtained through {1H,15N}-HMBC spectra at 15N natural abundance, unambiguously establish the coordination mode of cppH (viaNo or Np) in a series of Ru(ii) compounds.

1998 ◽  
Vol 53 (4) ◽  
pp. 411-415 ◽  
Author(s):  
Bernd Wrackmeyer ◽  
Ēriks Kupče

Abstract Ultrahigh resolution 15N NMR spectra were measured for two nitroalkanes (MeNO2 la, tBuNO2 1c), two isocyanates (tBuNCO 2c, Me3SiNCO 2d), four isothiocyanates (MeNCS 3a, EtNCS 3b, tBuNCS 3c, Me3SiNCS 3d), one carbodiimide (Me3SiNCNSiMe3 4d), one keteneimine [Me3SiNCC(SiMe3)2 5d], two sulphinyl imides (tBuNSO 6c, Me3SiNSO 6d), and N-tert-butyl-pyrrole 7c, in order to determine coupling constants J(15N ,I3C) and isotope induced chemical shifts 1∆12/13C (15N) at the natural abundance of the isotopes. The values 1∆12/13C (15N) can be separated into two groups, one dealing with NC single and another one with NC double bonds. In each group (with few exceptions), the values 1∆12/13C (15N) become more negative with a decrease in the absolute magnitude of l1J(l5N ,13C)l. The corresponding values 1∆14/15N (13C) show a sim ilar behaviour. However, N-substituted pyrroles appear to be exceptional in this respect.


2010 ◽  
Vol 113 (12) ◽  
pp. 573-574 ◽  
Author(s):  
Marcel H. P. van Genderen ◽  
Maurice W. P. L. Baars ◽  
Jan C. M. van Hest ◽  
E.W. Meijer ◽  
Ellen M. M. de Brabander-van den Berg

1987 ◽  
Vol 42 (6) ◽  
pp. 703-706 ◽  
Author(s):  
Bernd Wrackmeyer ◽  
Klaus Schamel ◽  
Karlheinz Guldner ◽  
Max Herberhold

AbstractThe inorganic ring system linked to the [Cr(CO)5] fragment [R = tBu (1), NH2 (2)], has been studied by reverse two-dimensional, 2D, 1H{15N} NMR spectroscopy. In solution, the exchange of the N-H hydrogen atoms is slow on the NMR time scale. Chemical shifts δ(1H), δ(13C), δ(31P), δ(15N) and coupling constants 1J(31P1H), 2J(31P13C), 1J(31P15N) are reported. In the case of 2, the reduced coupling constants 2K(31PN1H) and 1K(31P15N) have the same sign.


1978 ◽  
Vol 33 (9) ◽  
pp. 993-996 ◽  
Author(s):  
Joachim Müller

The 15N NMR spectra of HN3 and CIN3 solutions were recorded under triply labelled conditions. The chemical shifts and coupling constants are discussed with respect to the structure and in relation to other isoelectronic compounds.


Polyhedron ◽  
2002 ◽  
Vol 21 (21) ◽  
pp. 2099-2105 ◽  
Author(s):  
Saeed Ahmad ◽  
Anvarhusein A. Isab ◽  
Abdul Rahman Al-Arfaj ◽  
Alan P. Arnold

Sign in / Sign up

Export Citation Format

Share Document