| 词条 | Molecular mass | |||||||||||||
| 释义 |
Relative molecular mass or molecular weight is the mass of a molecule. It is calculated as the sum of the relative atomic masses of each constituent element multiplied by the number of atoms of that element in the molecular formula. The molecular mass of small to medium size molecules, measured by mass spectrometry, determines stoichiometry. For large molecules such as proteins, methods based on viscosity and light-scattering can be used to determine molecular mass when crystallographic data are not available. DefinitionsBoth atomic and molecular masses are usually obtained relative to the mass of the isotope 12C (carbon 12), which by definition[1] is equal to 12. For example, the molecular mass of methane, whose molecular formula is CH4, is calculated as follows:
A more proper term would be "relative molecular mass". However the adjective 'relative' is omitted as it is universally assumed that atomic and molecular masses are relative to the mass of 12C. Relative atomic and molecular mass values are dimensionless but are given the "unit" Dalton (formerly atomic mass unit) to indicate that the number is equal to the mass of one molecule divided by {{frac|1|12}} of the mass of one atom of 12C. The mass of 1 mol of substance is designated as molar mass. By definition, it has the unit gram. In the example above the atomic mass of carbon is given as 12.011, not 12. This is because naturally occurring carbon is a mixture of the isotopes 12C, 13C and 14C which have relative atomic masses of 12, 13 and 14 respectively. Moreover, the proportion of the isotopes varies between samples, so 12.011 is an average value. By contrast, there is less variation in naturally occurring hydrogen so the average atomic mass is known more precisely. The precision of the molecular mass is determined by precision of the least precise atomic mass value, in this case that of carbon. In high-resolution mass spectrometry the isotopomers 12C1H4 and 13C1H4 are observed as distinct molecules, with molecular masses of 16 and 17, respectively. The intensity of the mass-spectrometry peaks is proportional to the isotopic abundances in the molecular species. 12C 2H 1H3 can also be observed with molecular mass of 17. DeterminationMass spectrometry{{main|Mass spectrometry}}In mass spectrometry, the molecular mass of a small molecule is usually reported as the monoisotopic mass, that is, the mass of the molecule containing only the most common isotope of each element. Note that this also differs subtly from the molecular mass in that the choice of isotopes is defined and thus is a single specific molecular mass of the many possible. The masses used to compute the monoisotopic molecular mass are found on a table of isotopic masses and are not found on a typical periodic table. The average molecular mass is often used for larger molecules since molecules with many atoms are unlikely to be composed exclusively of the most abundant isotope of each element. A theoretical average molecular mass can be calculated using the standard atomic weights found on a typical periodic table, since there is likely to be a statistical distribution of atoms representing the isotopes throughout the molecule. This however may differ from the true average molecular mass of the sample due to natural (or artificial) variations in the isotopic distributions. Hydrodynamic methodsTo a first approximation, the basis for determination of molecular mass according to Mark–Houwink relations[2] is the fact that the intrinsic viscosity of solutions (or suspensions) of macromolecules depends on volumetric proportion of the dispersed particles in a particular solvent. Specifically, the hydrodynamic size as related to molecular mass depends on a conversion factor, describing the shape of a particular molecule. This allows the apparent molecular mass to be described from a range of techniques sensitive to hydrodynamic effects, including DLS, SEC (also known as GPC when the eluent is an organic solvent), viscometry, and diffusion ordered nuclear magnetic resonance spectroscopy (DOSY).[3] The apparent hydrodynamic size can then be used to approximate molecular mass using a series of macromolecule-specific standards.[4] As this requires calibration, it's frequently described as a "relative" molecular mass determination method. Static light scatteringIt is also possible to determine absolute molecular mass directly from light scattering, traditionally using the Zimm method. This can be accomplished either via classical static light scattering or via multi-angle light scattering detectors. Molecular masses determined by this method do not require calibration, hence the term "absolute". The only external measurement required is refractive index increment, which describes the change in refractive index with concentration. See also
References1. ^{{cite journal | author = International Union of Pure and Applied Chemistry | title = Atomic Weights of the Elements 1979 | url = http://www.iupac.org/publications/pac/1980/pdf/5210x2349.pdf | doi = 10.1351/pac198052102349 | journal = Pure Appl. Chem. | year = 1980 | volume = 52 | pages = 2349–84 | issue = 10}} 2. ^Paul, Hiemenz C., and Lodge P. Timothy. Polymer Chemistry. Second ed. Boca Raton: CRC P, 2007. 336, 338–339. 3. ^{{cite journal|author1=Johnson Jr., C. S. |journal=Progress in Nuclear Magnetic Resonance Spectroscopy|year=1999| volume=34|pages=203–256|title=Diffusion ordered nuclear magnetic resonance spectroscopy: principles and applications |doi=10.1016/S0079-6565(99)00003-5}} 4. ^{{cite journal|author1=Neufeld, R. |author2=Stalke, D. |journal=Chem. Sci.|year=2015| volume=6|pages=3354–3364|title=Accurate Molecular Weight Determination of Small Molecules via DOSY-NMR by Using External Calibration Curves with Normalized Diffusion Coefficients |doi=10.1039/C5SC00670H|url=http://goedoc.uni-goettingen.de/goescholar/bitstream/handle/1/11975/c5sc00670h.pdf?sequence=1}} {{open access}} External links
2 : Amount of substance|Mass |
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