I. Król-Starzomska,, A. Filarowski,, M. Rospenk, and, A. Koll, . Six and eight coordinate complexes of tin(IV) with some aromatic SCHIFF bases. Please note: If you switch to a different device, you may be asked to login again with only your ACS ID. B.S. High aspect ratio nanotubes assembled from macrocyclic iminium salts. La frequenza di stretching del legame C=C è più bassa nel caso degli aromatici (1500 cm-1) che non negli alcheni (1650 cm-1 circa). OH-substituted tridentate ONO Schiff base ligands and related molybdenum(VI) complexes for solvent-free (ep)oxidation catalysis with TBHP as oxidant. Temperature dependence of the CN stretching vibration of a nitrile-derivatized phenylalanine in water. Find more information about Crossref citation counts. Find more information about Crossref citation counts. on alkaloid from marine sponge The Nuclear Magnetic Resonance and Infrared Spectra of Aromatic Azomethines. Mehrotra. Structure de dithia-1,6a SIV AZA-6 pentalénes. Synthesis of poly-Schiff bases and some copper(II) and manganese(lI) polychelates. Journal of Molecular Catalysis A: Chemical. 15 publications. Banks. Vibrational study of p, p′-disubstituted N-benzylideneanilines. Lo spettro del n-esano mostra forti bande di assorbimento a 2900 cm-1 che sono il risultato dei movimenti di stiramento (stretching) dei legami C-H. A 1460 cm-1 abbiamo il bending  del CH2 e il bending asimmetrico del CH3, mentre a 1380 cm-1 si ha la deformazione simmetrica del CH3.  Poiché la zona 2000 - 1800 cm-1 è abbastanza sgombra sono facilmente visibili le cosiddette dita dellâaromatico, costituite da 2, 3 o 4 bande. The Altmetric Attention Score is a quantitative measure of the attention that a research article has received online. ScienceDirect ® is a registered trademark of Elsevier B.V. ScienceDirect ® is a registered trademark of Elsevier B.V. N.S. Marwa Belkhiria, Ali Mechria, Tiago F.C. Copper complexes of salicylidene anilines. Clicking on the donut icon will load a page at altmetric.com with additional details about the score and the social media presence for the given article. We use cookies to help provide and enhance our service and tailor content and ads. Stereoselective Bulk Synthesis of CCR2 Antagonist BMS-741672: Assembly of an All-cis (S,R,R)-1,2,4-Triaminocyclohexane (TACH) Core via Sequential Heterogeneous Asymmetric Hydrogenations. C=N: 2250-2100: weak-medium: C=C: stronger if near electronegative atoms: 1800-1600: strong: C=O: lower frequency (1650-1550) if attached to O or N middle frequency if attached to C, H higher frequency (1800) if attached to Cl: 1650-1450: weak-medium: C=C: lower frequency (1600-1450) if conjugated (i.e. Material taken from the Ph.D. thesis of R. Venkataraghavan to be submitted to the Indian Institute of Science under the guidance of C. N. R. Rao. A 1700 cm-1 si nota lâassorbimento del gruppo C=O. ScienceDirect ® is a registered trademark of Elsevier B.V. ScienceDirect ® is a registered trademark of Elsevier B.V. Structural information on some beryllium(II) complexes of N-aralkylsalicylaldimines. Karajagi, A.J. Yann Bernhard, Vivian Lioret, Richard A. Decréau. Copper complexes of salicylidene anilines. Summary: N–H stretch 3400-3250 cm-1. Complexes of tellurium with vanillydene-schiff bases. Copper(II), nickel(II) and cobalt(II) complexes of oxaldihydrazide and succindihydrazide Schiff bases with salicylaldehyde ando-hydroxyacetophenone. Callyspongia T.M. The increase in the CN(H) stretching frequency upon protonation is shown to be neither due to a negative CN/CNH coupling force constant nor due to the CN stretching but to be mainly due to the strong contribution from the large CNH bending force constant (1.08 mdyn/rad2) and a positive coupling constant (0.30 mdyn/rad). Patil. Due to the contributions of these two modes, the C=N stretching frequency is particularly sensitive to the magnitude of the Schiff base counterion interactions and to the hydrogen bonding environment of the Schiff base nitrogen. Copyright © 1967 Published by Elsevier B.V. Spectrochimica Acta Part A: Molecular Spectroscopy, https://doi.org/10.1016/0584-8539(67)80219-8.
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