Mass Spectrometry

isotope pattern

/ EYE-so-tope PAT-ern /

Imagine a family photo where most siblings are the same height, but a predictable few are a little taller because they happen to wear thicker shoes. Atoms come in such 'height' variants too — isotopes, which are the same element but slightly different mass — and because nature mixes them in fixed proportions, a molecule shows up not as one clean peak but as a small, patterned cluster.

An isotope pattern is the group of closely spaced peaks a single compound produces because its atoms include naturally occurring isotopes of different mass. For example, most carbon is carbon-12 but about one in a hundred is the heavier carbon-13, so any carbon-containing ion is accompanied by a smaller peak one mass unit higher. The relative heights of these peaks follow the natural abundances of the isotopes.

It matters because the shape of the cluster betrays what atoms are present: elements like chlorine and bromine leave unmistakable two-peak signatures, and counting carbons is possible from the size of the carbon-13 peak. The caveat is that isotope patterns become harder to read for very large molecules, where the peaks merge into a broad envelope, and for low-resolution instruments that cannot separate them cleanly.

A compound containing one chlorine atom shows two molecular-ion peaks two mass units apart in a roughly 3:1 ratio, because chlorine is about three-quarters chlorine-35 and one-quarter chlorine-37 — an instant giveaway that chlorine is present.

The pattern of isotope peaks reveals which elements a molecule contains.

The isotope pattern is set by nature's fixed isotope abundances, so it is predictable and can be calculated in advance for any proposed formula — comparing the observed cluster to the calculated one is a powerful check on a tentative identification.

Also called
isotopic distribution同位素图案同位素圖案同位素分布