Classification of rigid rotors: Difference between revisions

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:''See the main article: [[inertia moment]].''
:''See the main article: [[inertia moment]].''


The idea of a [[rigid rotor]] originates in classical mechanics, and finds a most important application in [[molecular physics]],  especially in [[microwave spectroscopy]]. This is the branch of spectroscopy that studies rotational transitions of molecules. In microwave spectroscopy molecules are regarded as rigid rotors in first approximation.
The definition of [[rigid rotor]] stems from classical mechanics. The concept is applied in [[molecular physics]],  especially in [[microwave spectroscopy]]. This is the branch of spectroscopy that studies rotational transitions of molecules. In microwave spectroscopy molecules are regarded as rigid rotors (in first approximation).


In classical mechanics, as well as quantum mechanics, the kinetic energy of rotation of a rigid rotor is linear in a quantity called the [[inertia tensor]]. This is a real, symmetric, 3 &times; 3 tensor which has three real eigenvalues: the ''principal moments of inertia'',<ref> Often the adjective ''principal'' is omitted, which is somewhat sloppy, because a moment of inertia can be defined with respect to any axis, and a principal moment is defined with respect to a principal axis. Following common usage we will drop the word ''principal'', however.</ref> denoted by ''I''<sub>''A''</sub>,  ''I''<sub>''B''</sub>,  ''I''<sub>''C''</sub>.   
In classical mechanics, as well as in quantum mechanics, the kinetic energy of rotation of a rigid rotor is linear in a quantity called the [[inertia tensor]]. This is a real, symmetric, 3 &times; 3 tensor which has three real eigenvalues: the ''principal moments of inertia'',<ref> Often the adjective ''principal'' is omitted, which is somewhat sloppy, because a moment of inertia can be defined with respect to any axis, and a principal moment is defined with respect to a principal axis. Following common usage we will drop the word ''principal'', however.</ref> denoted by ''I''<sub>''A''</sub>,  ''I''<sub>''B''</sub>,  ''I''<sub>''C''</sub>.   
The corresponding eigenvectors (the ''principal axes'') are orthogonal and have as common origin the center of mass of the rotor.
The corresponding eigenvectors (the ''principal axes'') are orthogonal and have as common origin the center of mass of the rotor.


==Classification of molecules based on inertia moments==
==Classification of molecules based on inertia moments==
The general convention is to define the axes such that the axis <math>A</math> has the smallest moment of inertia (and hence the highest rotational frequency) and other axes such that <math>I_A <= I_B <= I_C</math>. Sometimes the axis <math>A</math> may be associated with the symmetric axis of the molecule, if any. If such is the case, then <math>I_A</math> need not be the smallest moment of inertia. To avoid confusion, we will stick with the former  convention for the rest of the article. The particular pattern of [[energy level]]s (and hence of transitions in the rotational spectrum) for a molecule is determined by its symmetry. Depending on the relative size of the inertia moments, rotors can de divided into four classes.
The principal axes are ordered such that associated inertia moments decrease, that is, the ''A''-axis has the smallest moment of inertia and other axes are such that ''I''<sub>''A''</sub≤''I''<sub>''B''</sub> ≤ ''I''<sub>''C''</sub>. Depending on the relative size of the inertia moments, rotors can de divided into four classes.


===Linear rotors===
===Linear rotors===
For a linear molecule <math>I_A << I_B = I_C</math>. For most of the purposes, <math>I_A</math> is taken to be zero. For a linear molecule, the separation of lines in the rotational spectrum can be related directly to the moment of inertia of the molecule, and for a molecule of known atomic masses, can be used to determine the [[bond length]]s (structure) directly. For [[diatomic|diatomic molecules]] this process is trivial, and can be made from a single measurement of the rotational spectrum. For linear molecules with more atoms, rather more work is required, and it is necessary to measure molecules in which more than one isotope of each atom have been substituted (effectively this gives rise to a set of simultaneous equations which can be solved for the [[bond length]]s).
For a linear molecule ''I''<sub>''A''</sub> << ''I''<sub>''B''</sub> = ''I''<sub>''C''</sub>. For most purposes ''I''<sub>''A''</sub> can taken to be zero. For a linear molecule the separation of lines in the rotational spectrum can be related directly to the moment of inertia of the molecule. Since the moment of inertia is quadratic in the [[bond length]]s, the microwave spectrum yields the bond lengths directly, provided the atomic masses are known.  


Examples or linear molecules: [[Oxygen|Oxygen (O=O)]], [[Carbon monoxide|Carbon monoxide (O≡C<sup>*</sup>)]], [[Hydroxyl radical|Hydroxy radical (OH)]], [[Carbon dioxide|Carbon dioxide (O=C=O)]], [[Hydrogen cyanide|Hydrogen cyanide (HC≡N)]], [[Carbonyl sulfide|Carbonyl sulfide (O=C=S)]], [[chloroethyne|Chloroethyne (HC≡CCl)]], [[Acetylene|Acetylene (HC≡CH)]]
Examples of linear molecules are obviously the diatomics such as [[oxygen]] (O=O), [[carbon monoxide]] (C≡O), and [[nitrogen]] (N≡N). But also many triatoms are linear:
[[carbon dioxide]] (O=C=O), [[hydrogen cyanide]] (HC≡N), and  [[carbonyl sulfide]] (O=C=S). Examples of larger linear molecules are  [[chloroethyne]] (HC≡CCl), and [[acetylene]] (HC≡CH).
===Symmetric tops===
===Symmetric tops===
A symmetric top is a rotor in which two moments of inertia are the same. As a matter of historical convenience, spectroscopists divide molecules into two classes of symmetric tops, ''[[Oblate]] symmetric tops'' (saucer or disc shaped)  with <math>I_A = I_B < I_C</math> and ''[[Prolate]] symmetric tops'' (rugby football, or cigar shaped) with <math>I_A < I_B = I_C</math>. The spectra look rather different, and are instantly recognizable. As for linear molecules, the structure of ''symmetric tops'' ([[bond length]]s and [[Molecular geometry|bond angles]]) can be deduced from their spectra.  
A symmetric top is a rotor in which two moments of inertia are the same. Spectroscopists divide molecules into two classes of symmetric tops, ''oblate symmetric tops'' (frisbee or disc shaped)  with ''I''<sub>''A''</sub> = ''I''<sub>''B''</sub> < ''I''<sub>''C''</sub> and ''prolate symmetric tops'' (cigar shaped) with ''I''<sub>''A''</sub> < ''I''<sub>''B''</sub> = ''I''<sub>''C''</sub>.
Symmetric tops  have a three-fold or higher rotational symmetry axis.


Examples of symmetric tops:  
Examples of oblate symmetric tops are: [[benzene]] (C<sub>6</sub>H<sub>6</sub>), [[cyclobutadiene]] (C<sub>4</sub>H<sub>4</sub>), and [[ammonia]] (NH<sub>3</sub>). Prolate tops are: [[chloroform]](CHCl<sub>3</sub>) and [[methylacetylene]] (CH<sub>3</sub>C≡CH).
* [[Oblate]]: [[Benzene|Benzene (C<sub>6</sub>H<sub>6</sub>)]], [[Cyclobutadiene|Cyclobutadiene (C<sub>4</sub>H<sub>4</sub>)]], [[Ammonia|Ammonia (NH<sub>3</sub>)]]
* [[Prolate]]: [[Chloroform|Chloroform (CHCl<sub>3</sub>)]], [[Methylacetylene|Propyne (CH<sub>3</sub>C≡CH)]]
===Spherical tops===
===Spherical tops===
A spherical top molecule, can be considered as a special case of ''symmetric tops'' with equal moment of inertia about all three axes (<math>I_A = I_B = I_C</math>).
A spherical top molecule is a special case of a symmetric tops with equal moment of inertia about all three axes ''I''<sub>''A''</sub> = ''I''<sub>''B''</sub> = ''I''<sub>''C''</sub>. The spherical  top molecules have [[cubic symmetry]].


Examples of spherical tops: [[Phosphorus tetramer|Phosphorus tetramer (P<sub>4</sub>)]], [[Carbon tetrachloride|Carbon tetrachloride (CCl<sub>4</sub>)]], [[Nitrogen tetrahydride|Nitrogen tetrahydride (NH<sub>4</sub>)]], [[Ammonium|Ammonium ion (NH<sub>4</sub><sup>+</sup>)]], [[Sulfur hexafluoride|Sulfur hexafluoride (SF<sub>6</sub>)]]
Examples of spherical tops are: [[methane]] (CH<sub>4</sub>), [[phosphorus tetramer]] (P<sub>4</sub>), [[carbon tetrachloride]] (CCl<sub>4</sub>), [[ammonium ion]] (NH<sub>4</sub><sup>+</sup>), and [[uranium hexafluoride]] (UF<sub>6</sub>).
===Asymmetric tops===
===Asymmetric tops===
A rotos is an asymmetric top if all three moments of inertia are different. Most of the larger molecules are asymmetric tops, even when they have a high degree of symmetry. Generally for such molecules a simple interpretation of the spectrum is not normally possible. Sometimes asymmetric tops have spectra that are similar to those of a linear molecule or a symmetric top, in which case the molecular structure must also be similar to that of a linear molecule or a symmetric top. For the most general case, however, all that can be done is to fit the spectra to three different moments of inertia. If the molecular formula is known, then educated guesses can be made of the possible structure, and from this guessed structure, the moments of inertia can be calculated. If the calculated moments of inertia agree well with the measured moments of inertia, then the structure can be said to have been determined. For this approach to determining molecular structure, isotopic substitution is invaluable.  
A rotor is an asymmetric top if all three moments of inertia are different. Most of the larger molecules are asymmetric tops. For such molecules a simple interpretation of the microwave spectrum usually is not possible. Sometimes asymmetric tops have rotational spectra that are similar to those of a linear molecule or a symmetric top, in which case the molecular structure must also be similar to that of a linear molecule or a symmetric top. In the determination of the molecular structure of asymmetric tops from microwave spectrum, [[isotopic substitution]] is invaluable.  


Examples of asymmetric tops: [[Anthracene|Anthracene (C<sub>14</sub>H<sub>10</sub>)]], [[Water (molecule)|Water (H<sub>2</sub>O)]], [[Nitrogen dioxide|Nitrogen dioxide (NO<sub>2</sub>)]]
Examples of asymmetric tops: [[anthracene]] (C<sub>14</sub>H<sub>10</sub>), [[water]]  (H<sub>2</sub>O), and  [[nitrogen dioxide]] (NO<sub>2</sub>).
==Note==
==Note==
<references />
<references />

Revision as of 09:50, 18 September 2007

It is possible, and customary in microwave spectroscopy, to classify rigid rotors by the relative size of their principal moments of inertia.

Inertia moment

See the main article: inertia moment.

The definition of rigid rotor stems from classical mechanics. The concept is applied in molecular physics, especially in microwave spectroscopy. This is the branch of spectroscopy that studies rotational transitions of molecules. In microwave spectroscopy molecules are regarded as rigid rotors (in first approximation).

In classical mechanics, as well as in quantum mechanics, the kinetic energy of rotation of a rigid rotor is linear in a quantity called the inertia tensor. This is a real, symmetric, 3 × 3 tensor which has three real eigenvalues: the principal moments of inertia,[1] denoted by IA, IB, IC. The corresponding eigenvectors (the principal axes) are orthogonal and have as common origin the center of mass of the rotor.

Classification of molecules based on inertia moments

The principal axes are ordered such that associated inertia moments decrease, that is, the A-axis has the smallest moment of inertia and other axes are such that IAIBIC. Depending on the relative size of the inertia moments, rotors can de divided into four classes.

Linear rotors

For a linear molecule IA << IB = IC. For most purposes IA can taken to be zero. For a linear molecule the separation of lines in the rotational spectrum can be related directly to the moment of inertia of the molecule. Since the moment of inertia is quadratic in the bond lengths, the microwave spectrum yields the bond lengths directly, provided the atomic masses are known.

Examples of linear molecules are obviously the diatomics such as oxygen (O=O), carbon monoxide (C≡O), and nitrogen (N≡N). But also many triatoms are linear: carbon dioxide (O=C=O), hydrogen cyanide (HC≡N), and carbonyl sulfide (O=C=S). Examples of larger linear molecules are chloroethyne (HC≡CCl), and acetylene (HC≡CH).

Symmetric tops

A symmetric top is a rotor in which two moments of inertia are the same. Spectroscopists divide molecules into two classes of symmetric tops, oblate symmetric tops (frisbee or disc shaped) with IA = IB < IC and prolate symmetric tops (cigar shaped) with IA < IB = IC. Symmetric tops have a three-fold or higher rotational symmetry axis.

Examples of oblate symmetric tops are: benzene (C6H6), cyclobutadiene (C4H4), and ammonia (NH3). Prolate tops are: chloroform(CHCl3) and methylacetylene (CH3C≡CH).

Spherical tops

A spherical top molecule is a special case of a symmetric tops with equal moment of inertia about all three axes IA = IB = IC. The spherical top molecules have cubic symmetry.

Examples of spherical tops are: methane (CH4), phosphorus tetramer (P4), carbon tetrachloride (CCl4), ammonium ion (NH4+), and uranium hexafluoride (UF6).

Asymmetric tops

A rotor is an asymmetric top if all three moments of inertia are different. Most of the larger molecules are asymmetric tops. For such molecules a simple interpretation of the microwave spectrum usually is not possible. Sometimes asymmetric tops have rotational spectra that are similar to those of a linear molecule or a symmetric top, in which case the molecular structure must also be similar to that of a linear molecule or a symmetric top. In the determination of the molecular structure of asymmetric tops from microwave spectrum, isotopic substitution is invaluable.

Examples of asymmetric tops: anthracene (C14H10), water (H2O), and nitrogen dioxide (NO2).

Note

  1. Often the adjective principal is omitted, which is somewhat sloppy, because a moment of inertia can be defined with respect to any axis, and a principal moment is defined with respect to a principal axis. Following common usage we will drop the word principal, however.