应《网络安全法》要求，自2017年10月1日起，未进行实名认证将不得使用互联网跟帖服务。为保障您的帐号能够正常使用，请尽快对帐号进行手机号验证，感谢您的理解与支持！

24小时热门版块排行榜    

小木虫论坛-学术科研互动平台 » 计算模拟区 » 量子化学 » 量化新手直通车 » 【求助】电子态1Δg，1∑+g，2p等怎么定义的，
51/1返回列表
查看: 2362  |  回复: 8
只看楼主 @他人 存档 新回复提醒 (忽略) 收藏    在APP中查看
当前只显示满足指定条件的回帖，点击这里查看本话题的所有回帖

zhang302

新虫 (初入文坛)

[交流] 【求助】电子态1Δg，1∑+g，2p等怎么定义的，

我最近看文献，一直看到这个。实在有点不明白这些电子态是什么意思。只知道它是电子态。望大侠们给我解析一下，必有重金酬谢
其他电子态的说明也可以在下面留言，与前几个电子态一视同仁，金币不是问题
求讲解
越详细越好
回复此楼

» 猜你喜欢

» 本主题相关价值贴推荐，对您同样有帮助:

» 抢金币啦！回帖就可以得到:

查看全部散金贴
1楼 2011-03-31 10:17:39
已阅   回复此楼   关注TA 给TA发消息 送TA红花 TA的回帖

zhang302

新虫 (初入文坛)
引用回帖:
Originally posted by physics7778 at 2011-03-31 11:39:19:
建议你去看《分子光谱与分子结构》第一卷 双原子分子光谱 【加】G.赫兹堡  著
第六章  构造原理、电子组态和化学价。书上讲的很清楚。有需要可以传给你电子版的。

如果能帮我贴出来更好，呵呵
赞一下 回复此楼
3楼2011-03-31 15:37:45
已阅   回复此楼   关注TA 给TA发消息 送TA红花 TA的回帖
查看全部 9 个回答

physics7778

木虫 (正式写手)

建议

★ ★
zhang302(金币+5): 提供了一个明确的查阅途径 2011-03-31 15:36:29
小红豆(金币+2): 谢谢分享你的看法 2011-04-16 14:06:28
引用回帖:
Originally posted by zhang302 at 2011-03-31 10:17:39:
我最近看文献，一直看到这个。实在有点不明白这些电子态是什么意思。只知道它是电子态。望大侠们给我解析一下，必有重金酬谢
其他电子态的说明也可以在下面留言，与前几个电子态一视同仁，金币不是问题
求讲解
...

建议你去看《分子光谱与分子结构》第一卷 双原子分子光谱 【加】G.赫兹堡  著
第六章  构造原理、电子组态和化学价。书上讲的很清楚。有需要可以传给你电子版的。
赞一下(2人) 回复此楼
2楼2011-03-31 11:39:19
已阅   回复此楼   关注TA 给TA发消息 送TA红花 TA的回帖

yongma2008

木虫 (著名写手)
★ ★
zhang302(金币+10): 很感谢呀，我是不太会用度娘 2011-04-01 09:11:58
小红豆(金币+2): 谢谢分享你的看法 2011-04-16 14:06:39
引用回帖:
Originally posted by zhang302 at 2011-03-31 08:37:45:
如果能帮我贴出来更好，呵呵

其实度娘真的很有用，动动手啥都有了

http://good.gd/1081561.htm
赞一下(1人) 回复此楼
4楼2011-03-31 19:51:38
已阅   回复此楼   关注TA 给TA发消息 送TA红花 TA的回帖

jmlong

木虫 (正式写手)
★ ★ ★ ★ ★
zhang302(金币+10): 2011-04-01 09:10:58
小红豆(金币+5): 谢谢分享你的看法 2011-04-16 14:07:04
In molecular physics, the molecular term symbol is a shorthand expression of the group representation and angular momenta that characterize the state of a molecule, i.e. its electronic quantum state which is an eigenstate of the electronic molecular Hamiltonian. It is the equivalent of the term symbol for the atomic case. However, the following presentation is restricted to the case of homonuclear diatomic molecules, or symmetric molecules with an inversion centre. For heteronuclear diatomic molecules, the u/g  symbol does not correspond to any exact symmetry of the electronic molecular Hamiltonian. In the case of less symmetric molecules the molecular term symbol contains the symbol of the group representation to which the molecular electronic state belongs.

It has the general form:


where

    * S is the total spin quantum number
    * Λ is the orbital angular momentum along the internuclear axis
    * Ω is the total angular momentum along the internuclear axis
    * u/g is the parity
    * +/− is the reflection symmetry along an arbitrary plane containing the internuclear axis

For atoms, we use S, L, J and MJ to characterize a given state. In linear molecules, however, the lack of spherical symmetry destroys the relationship [\hat\mathbf L^2, \hat H]=0, so L ceases to be a good quantum number. A new set of operators have to be used instead: \{\hat \mathbf S^2, \hat\mathbf{S}_z, \hat\mathbf{L}_z, \hat\mathbf{J}_z=\hat\mathbf{S}_z + \hat\mathbf{L}_z\}, where the z-axis is defined along the internuclear axis of the molecule. Since these operators commute with each other and with the Hamiltonian  on the limit of negligible spin-orbit coupling, their eigenvalues may be used to describe a molecule state through the quantum numbers S, MS, ML and MJ.

The cylindrical symmetry of a linear molecule ensures that positive and negative values of a given ml for an electron in a molecular orbital will be degenerate in the absence of spin-orbit coupling. Different molecular orbitals are classified with a new quantum number, λ, defined as

    λ = |ml|

Following the spectroscopic notation pattern, molecular orbitals are designated by a smallcase Greek letter: for λ = 0, 1, 2, 3,… orbitals are called σ, π, δ, φ… respectively.

Now, the total z-projection of L can be defined as

    M_L=\sum_i {m_l}_i.

As states with positive and negative values of ML are degenerate, we define

    Λ = |ML|,

and a capital Greek letter is used to refer to each value: Λ = 0, 1, 2, 3… are coded as Σ, Π, Δ, Φ… respectively. The molecular term symbol is then defined as

    2S+1Λ

and the number of electron degenerate states (under the absence of spin-orbit coupling) corresponding to this term symbol is given by:

    * (2S+1)×2 if Λ is not 0
    * (2S+1) if Λ is 0.

Ω and spin-orbit coupling

Spin-orbit coupling lifts the degeneracy of the electronic states. This is because the z-component of spin interacts with the z-component of the orbital angular momentum, generating a total electronic angular momentum along the molecule axis Jz. This is characterized by the MJ quantum number, where

    MJ = MS + ML.

Again, positive and negative values of MJ are degenerate, so the pairs (ML, MS) and (−ML, −MS) are degenerate: {(1, 1/2), (−1, −1/2)}, and {(1, −1/2), (−1, 1/2)} represent two different degenerate states. These pairs are grouped together with the quantum number Ω, which is defined as the sum of the pair of values (ML, MS) for which ML is positive. Sometimes the equation

    Ω = Λ + MS

is used (often Σ is used instead of MS). Note that although this gives correct values for Ω it could be misleading, as obtained values do not correspond to states indicated by a given pair of values (ML,MS). For example, a state with (−1, −1/2) would give an Ω value of Ω = |−1| + (−1/2) = −1/2, which is wrong. Choosing the pair of values with ML positive will give a Ω = 3/2 for that state.

With this, a level is given by

    2S + 1ΛΩ

Note that Ω can have negative values and subscripts r and i represent regular (normal) and inverted multiplets, respectively.[1] For a 4Π term there are four degenerate (ML, MS) pairs: {(1, 3/2), (−1, −3/2)}, {(1, 1/2), (−1, −1/2)}, {(1, −1/2), (−1, 1/2)}, {(1, −3/2), (−1, 3/2)}. These correspond to Ω values of 5/2, 3/2, 1/2 and −1/2, respectively. Approximating the spin-orbit Hamiltonian to first order perturbation theory, the energy level is given by

    E = A ML MS

where A is the spin-orbit constant. For 4Π the Ω values 5/2, 3/2, 1/2 and −1/2 correspond to energies of 3A/2, A/2, −A/2 and −3A/2. Despite of having the same magnitude, levels of Ω = ±1/2 have different energies associated, so they are not degenerate. With that convention, states with different energies are given different Ω values. For states with positive values of A (which are said to be regular), increasing values of Ω correspond to increasing values of energies; on the other hand, with A negative (said to be inverted) the energy order is reversed. Including higher order effects can lead to a spin-orbital levels or energy that do not even follow the increasing value of Ω.

When Λ = 0 there is no spin-orbit splitting to first order in perturbation theory, as the associated energy is zero. So for a given S, all of its MS values are degenerate. This degeneracy is lifted when spin-orbit interaction is treated to higher order in perturbation theory, but still states with same |MS| are degenerate in a non-rotating molecule. We can speak of a 5Σ2 substate, a 5Σ1 substate or a 5Σ0 substate. Except for the case Ω = 0, these substates have a degeneracy of 2.


Reflection through a plane containing the internuclear axis

There are an infinite number of planes containing the internuclear axis and hence there are an infinite number of possible reflexions. For any of these planes, molecular terms with Λ > 0 always have a state which is symmetric with respect to this reflection and one state that is antisymmetric. Rather than labelling those situations as, e.g., 2Π±, the ± is omitted.

For the Σ states, however, this two-fold degeneracy disappears, and all Σ states are either symmetric under any plane containing the internuclear axis, or antisymmetric. These two situations are labeled as Σ+ or Σ−.

Reflection through an inversion center: u and g symmetry

Taking the molecule center of mass as origin of coordinates, consider the change of all electrons’ position from (xi, yi, zi) to (−xi, −yi, −zi). If the resulting wave function is unchanged, it is said to be gerade (German for even); if the wave function changes sign then it is said to be ungerade (odd). For a molecule with a center of inversion, all orbitals will be symmetric or antisymmetric. The resulting wavefunction for the whole multielectron system will be gerade if an even number of electrons is in [[ungerade orbitals]], and ungerade if there is an odd number of electrons in ungerade orbitals, independently of the number of electrons in gerade orbitals.

[ Last edited by jmlong on 2011-4-1 at 06:09 ]
赞一下(2人) 回复此楼
5楼2011-04-01 06:01:35
已阅   回复此楼   关注TA 给TA发消息 送TA红花 TA的回帖
查看全部 9 个回答
普通表情 龙 兔 虎 猫 高级回复 (可上传附件)
信息提示
关闭
请填处理意见
关闭