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Chemical shift

About: Chemical shift is a research topic. Over the lifetime, 23316 publications have been published within this topic receiving 337653 citations.


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TL;DR: The use of absolute magnetic shieldings, computed at ring centers with available quantum mechanics programs, are proposed as a new aromaticity/antiaromaticity criterion to establish NICS as an effective aromaticity criterion.
Abstract: The ability to sustain a diatropic ring current is the defining characteristic of aromatic species.1-7 Cyclic electron delocalization results in enhanced stability, bond length equalization, and special magnetic as well as chemical and physical properties.1 In contrast, antiaromatic compounds sustain paratropic ring currents3 despite their localized, destabilized structures.1-7 We have demonstrated the direct, quantitative relationships among energetic, geometrical, and magnetic criteria of aromaticity in a wide-ranging set of aromatic/antiaromatic fivemembered rings.5a While the diamagnetic susceptibility exaltation (Λ) is uniquely associated with aromaticity, it is highly dependent on the ring size (area2) and requires suitable calibration standards.6 Aromatic stabilization energies (ASEs) of strained and more complicated systems are difficult to evaluate. CC bond length variations in polybenzenoid hydrocarbons can be just as large as those in linear conjugated polyenes.2 The abnormal proton chemical shifts of aromatic molecules are the most commonly employed indicators of ring current effects.1 However, the ca. 2-4 ppm displacements of external protons to lower magnetic fields are relatively modest (e.g., δH ) 7.3 for benzene vs 5.6 for dC-H in cyclohexene). In contrast, the upfield chemical shifts of protons located inside aromatic rings are more unusual. The six inner hydrogens of [18]annulene, for example, resonate at -3.0 ppm vs δ ) 9.28 for the outer protons. This relationship is inverted dramatically in the antiaromatic [18]annulene dianion, C18H18, where δ ) 20.8 and 29.5 (in) vs. -1.1 (out).8 Similar demonstrations of paratropic ring currents in antiaromatic compounds are well documented.3,8,9 Chemical shifts of encapsulated 3He atoms are now employed as experimental and computed measures of aromaticity in fullerenes and fullerene derivatives.10 While the rings of most aromatic systems are too small to accommodate atoms internally, the chemical shifts of hydrogens in bridging positions have long been used as aromaticity and antiaromaticity probes.9 δLi+ can be employed similarly, with the advantage that Li+ complexes with individual rings in polycyclic systems can be computed.4,11 We now propose the use of absolute magnetic shieldings, computed at ring centers (nonweighted mean of the heavy atom coordinates) with available quantum mechanics programs,12 as a new aromaticity/antiaromaticity criterion. To correspond to the familiar NMR chemical shift convention, the signs of the computed values are reversed: Negative “nucleus-independent chemical shifts” (NICSs) denote aromaticity; positive NICSs, antiaromaticity (see Table 1 for selected results). Figure 1, a plot of NICSs vs the ASEs for our set of five-membered ring heterocycles,5a provides calibration. The equally good correlations with magnetic susceptibility exaltations and with structural variations establish NICS as an effective aromaticity criterion. Unlike Λ,6 NICS values for [n]annulenes (Table 1) show only a modest dependence on ring size. The 10 π electron systems give significantly higher values than those with 6 π electrons. The antiaromatic 4n π electron compounds, cyclobutadiene (27.6), pentalene (18.1), heptalene (22.7), and planar D4h cyclooctatetraene (30.1), all show highly positive NICSs. Like the Li+-complex probe,4 the NICS evaluates the aromaticity and antiaromaticity contributions of individual rings in polycyclic systems. Scheme 1 (HF/6-31+G*, data from Table 1) shows NICSs for selected examples. The benzenoid aromatic NICSs provide evidence both for localized and “perimeter” models. The naphthalene (1) NICS (-9.9) resembles that of benzene (-9.7), as do the NICSs for the outer rings of phenanthrene (2) (-10.2) and triphenylene (3); the aromaticity of the central rings of the latter two are reduced. The NICS of the central ring of anthracene (4) (-13.3) exceeds the benzene value in contrast to the outer ring NICS (-8.2). Remarkably, the NICS (-7.0) for the seven-membered ring of azulene (5) is very close to that of the tropylium ion (-7.6 ppm), whereas the azulene five-membered ring NICS (-19.7) is even larger in magnitude than that of the cyclopentadienyl anion (-14.3). The four-membered rings in benzocyclobutadiene (6) (NICS ) 22.5) and in biphenylene (7) (19.0) are antiaromatic, but less so than cyclobutadiene itself (27.6). The six-membered rings in these polycycles are still aromatic, but their NICSs (-2.5 (1) (a) Minkin, V. I.; Glukhovtsev, M. N.; Simkin, B. Y. Aromaticity and Antiaromaticity; Wiley: New York, 1994. (b) Garratt, P. J. Aromaticity; Wiley: New York, 1986. (c) Eluidge, J. A.; Jackman, L. M. J. Chem. Soc. 1961, 859. (2) Schleyer, P. v. R.; Jiao, H. Pure Appl. Chem. 1996, 28, 209. (3) Pople, J. A.; Untch, K. G. J. Am. Chem. Soc. 1966, 88, 4811. (4) Jiao, H; Schleyer, P. v. R. AIP Conference Proceedings 330, E.C.C.C.1, Computational Chemistry; Bernardi, F., Rivail, J.-L., Eds.; American Institute of Physics: Woodbury, New York, 1995; p 107. (5) (a) Schleyer, P. v. R.; Freeman, P.; Jiao, H.; Goldfuss, B. Angew. Chem., Int. Ed. Engl. 1995, 34, 337. (b) Jiao, H.; Schleyer, P. v. R. Unpublished IGLO results. (c) Kutzelnigg, W.; Fleischer, U.; Schindler, M. In NMR: Basic Princ. Prog.; Springer: Berlin, 1990; Vol. 23, p 165. (6) Dauben, H. J., Jr.; Wilson, J. D.; Laity, J. L. In Non-Benzenoid Aromatics; Synder, J., Ed.; Academic Press, 1971; Vol. 2, and references cited. The partitioning of ring current or ring current susceptabilitites among various rings in polycyclic syestems were considered earlier, e.g., by Aihara (Aihara, J. J. Am. Chem. Soc. 1985, 207, 298 and refs cited) and by Mallion (Haigh, C. W.; Mallion, J. Chem. Phys. 1982, 76, 1982). (7) Fleischer, U.; Kutzelnigg, W.; Lazzeretti, P.; Mühlenkamp, V. J. Am. Chem. Soc. 1994, 116, 5298. (8) Sondheimer, F. Acc. Chem. Res. 1972, 5, 81. (9) (a) Hunandi, R. J. J. Am. Chem. Soc. 1983, 105, 6889. (b) Pascal, R. A., Jr.; Winans, C. G.; Van Engen, D. J. Am. Chem. Soc. 1989, 111, 3007. (10) (a) Bühl, M.; Thiel, W.; Jiao, H.; Schleyer, P. v. R.; Saunders, M.; Anet, F. A. L. J. Am. Chem. Soc. 1994, 116, 7429 and references cited. (b) Bühl, M.; van Wüllen, C. Chem. Phys. Lett. 1995, 247, 63. The authors have shown that the negative absolute shielding in the center of C60 is nearly the same as δ3He, computed at the same level. (11) Paquette, L. A.; Bauer, W.; Sivik, M. R.; Bühl, M.; Feigel, M.; Schleyer, P. v. R. J. Am. Chem. Soc. 1990, 112, 8776. (12) Frisch, M. J.; Trucks, G. W.; Schlegel, H. B.; Gill, P. M. W.; Johnson, B. G.; Robb, M. A.; Cheeseman, J. R.; Keith, T. A.; Petersson, G. A.; Montgomery, J. A.; Raghavachari, K.; Al-Laham, M. A.; Zakrewski, V. G.; Ortiz, J. V.; Foresman, J. B.; Cioslowski, J.; Stefanov, B. B.; Nanayakkara, A.; Challacombe, M.; Peng, C. Y.; Ayala, P. Y.; Chen, W.; Wong, M. W.; Andres, J. L.; Replogle, E. S.; Gomperts, R.; Stewart, J. P.; Head-Gordon, M.; Gonzalez, C.; Pople, J. A. Gaussian 94, ReVision B.2; Gaussian Inc., Pittsburgh, PA, 1995. Figure 1. Plot of NICSs (ppm) vs the aromatic stabilization energies (ASEs, kcal/mol)5a for a set of five-membered ring heterocycles, C4H4X (X ) as shown) (cc ) 0.966). 6317 J. Am. Chem. Soc. 1996, 118, 6317

4,921 citations

Book
07 Mar 2008
TL;DR: In this paper, the authors present an overview of the basic concepts of one-dimensional NMR, including spin spin-spin coupling, spin-spin coupling, Heteronuclear coupling with other nuclei, and 13C coupling constants.
Abstract: 1. Molecular Formulas and What Can Be Learned from Them. 2. Infrared Spectroscopy. 3. Nuclear Magnetic Resonance Spectroscopy Part One: Basic Concepts. 4. Nuclear Magnetic Resonance Spectroscopy Part Two: Carbon-13 Spectra, Including Heteronuclear Coupling with Other Nuclei. 5. Nuclear Magnetic Resonance Spectroscopy Part Three: Spin-Spin Coupling. 6. Nuclear Magnetic Resonance Spectroscopy Part Four: Other Topics in One-Dimensional NMR. 7. Ultraviolet Spectroscopy. 8. Mass Spectrometry. 9. Combined Structure Problems. 10. Nuclear Magnetic Resonance Spectroscopy Part Five: Advanced NMR Techniques. Answers to Selected Problems. Appendix 1: Infrared Absorption Frequencies of Functional Groups. Appendix 2: Some Representative Chemical Shift Values for Various Types of Protons. Appendix 3: Typical Proton Coupling Constants. Appendix 4: Calculation of Proton (1H) Chemical Shifts. Appendix 5: Calculation of Carbon-13 Chemical Shifts. Appendix 6: 13C Coupling Constants. Appendix 7: Tables of Precise Masses and Isotopic Abundance Ratios for Molecular Ions Under Mass 100 Containing Carbon, Hydrogen, Nitrogen, and Oxygen. Appendix 8: Common Fragment Ions Under Mass 105. Appendix 9: Handy-Dandy Guide to Mass Spectral Fragmentation Patterns. Appendix 10: Index of Spectra.

2,543 citations

Journal ArticleDOI
TL;DR: In this paper, a considerable degree of variability exists in the way that 1H, 13C and 15N chemical shifts are reported and referenced for biomolecules and the authors explore some of the reasons for this situation and propose guidelines for future chemical shift referencing and for conversion from many common 1H and 13C chemical shift standards, now used in biomolecular NMR, to those proposed here.
Abstract: A considerable degree of variability exists in the way that 1H, 13C and 15N chemical shifts are reported and referenced for biomolecules. In this article we explore some of the reasons for this situation and propose guidelines for future chemical shift referencing and for conversion from many common 1H, 13C and 15N chemical shift standards, now used in biomolecular NMR, to those proposed here.

2,137 citations


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Performance
Metrics
No. of papers in the topic in previous years
YearPapers
2023111
2022276
2021172
2020198
2019161
2018200