8.2
Espectroscopia de RMN: Descripción general del cambio químico
La posición de la señal de absorción de una muestra se informa en relación con la posición de la señal de tetrametilsilano (TMS), que se agrega como r…
La posición de la frecuencia de absorción de RMN se expresa en términos de cuánto se desplaza de la señal de un compuesto de referencia, generalmente TMS.
La diferencia de frecuencia se divide por la frecuencia de funcionamiento del instrumento para producir el desplazamiento químico, una cantidad adimensional.
Expresados en partes por millón o ppm, los cambios químicos generalmente se trazan en la escala δ, donde la señal TMS aparece a 0 ppm.
Por ejemplo, la frecuencia de absorción de los protones de benceno es 436 hercios más alta que la señal TMS en un espectrómetro de 60 megahercios, mientras que la diferencia es de 2181 hercios en un instrumento de 300 megahercios.
El desplazamiento químico es de 7,27 ppm en ambos casos, lo que lo hace independiente de la frecuencia de funcionamiento del instrumento.
Las señales en el lado derecho del espectro son señales de campo ascendente de baja frecuencia que surgen de los núcleos blindados de entornos densos en electrones.
Por el contrario, las señales de la izquierda son señales de campo descendente de alta frecuencia de núcleos desblindados en entornos pobres en electrones.
View the full transcript and gain access to JoVE Core videos
Q1: Why is chemical shift expressed in parts per million rather than hertz?
Chemical shift is expressed in parts per million because it is a dimensionless quantity independent of the spectrometer's operating frequency. The frequency difference between a sample and TMS reference is divided by the instrument operating frequency, making the result consistent across different spectrometers. For example, benzene shows 436 Hz difference at 60 MHz and 2181 Hz at 300 MHz, yet both yield 7.27 ppm.
Q2: What does the δ scale represent in NMR spectroscopy?
The δ scale is the standard scale for reporting chemical shift values in parts per million. Tetramethylsilane (TMS), the reference compound, appears at 0 ppm on the δ scale. All sample signals are positioned relative to this reference point, allowing chemists to identify and compare nuclei based on their electronic environments.
Q3: How do shielded and deshielded nuclei appear on an NMR spectrum?
Shielded nuclei in electron-dense environments produce low-frequency upfield signals appearing on the right side of the spectrum at lower chemical shift values. Deshielded nuclei in electron-poor settings produce high-frequency downfield signals on the left side at higher chemical shift values. This spatial separation allows identification of different nuclear environments within a molecule.
Q4: Why does the frequency difference between sample and reference change with spectrometer strength?
The frequency difference changes because NMR absorption frequencies are directly proportional to the magnetic field strength of the spectrometer. A 300 MHz instrument operates at five times the field strength of a 60 MHz instrument, causing proportionally larger frequency differences. However, dividing by the operating frequency yields the same dimensionless chemical shift value.
Q5: What role does tetramethylsilane play in chemical shift determination?
Tetramethylsilane (TMS) serves as the internal reference standard for NMR spectroscopy, appearing at 0 ppm on the δ scale. All sample absorption frequencies are measured relative to the TMS signal, allowing consistent comparison of chemical shifts across different instruments and experiments. This standardization is essential for reproducible spectral interpretation.
Q6: How does electron density around a nucleus affect its chemical shift position?
Electron density directly influences chemical shift through shielding effects. Nuclei surrounded by electron-dense environments are shielded from the magnetic field, producing upfield signals at lower ppm values. Conversely, nuclei in electron-poor environments are deshielded, producing downfield signals at higher ppm values. This relationship enables identification of functional groups and structural features.
Q7: What calculation converts raw frequency data into chemical shift values?
Chemical shift is calculated by dividing the frequency difference between the sample and TMS reference (in hertz) by the spectrometer operating frequency (in megahertz), yielding a dimensionless quantity expressed in parts per million. This formula ensures that chemical shift values remain constant regardless of the instrument's magnetic field strength, enabling universal spectral comparison.