Explain the color in coordination compounds.

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(N/A) The color of coordination compounds is a major property of transition metal complexes. When white light passes through a sample,some part of it is absorbed. Therefore,the transmitted light is not white.
The color of the complex is the complementary color of the light absorbed. The complementary color is the color generated by the remaining wavelengths. For example,if green light is absorbed by the complex,it appears red. The relationship between the absorbed wavelength and the observed color is well-defined.
The color in coordination compounds can be explained in terms of Crystal Field Theory $(CFT)$.
Consider the complex $[Ti(H_2O)_6]^{3+}$,which is purple in color. This complex has a single electron $(3d^1)$ in the ground state occupying the $t_{2g}$ orbital. The next higher energy level available for the electron is the empty $e_g$ orbital.
If the complex absorbs light corresponding to the blue-green region,the electron is excited from the $t_{2g}$ level to the $e_g$ level.
$(t_{2g}^1 e_g^0 \rightarrow t_{2g}^0 e_g^1)$
As a result,the complex appears purple. This phenomenon is known as $d-d$ transition.

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Similar Questions

Given below are two statements: Statement $I$: Each electron in $e_g$ orbitals destabilizes the orbitals by $+0.6\Delta_o$ and each electron in the $t_{2g}$ orbitals stabilizes the orbitals by $-0.4\Delta_o$ in an octahedral field on the basis of crystal field theory. Statement $II$: All the $d$-orbitals of the transition metals have the same energy in their free atomic state but when a complex is formed the ligands destroy the degeneracy of these orbitals on the basis of crystal field theory. In the light of the above statements, choose the correct answer from the options given below:

What is the color of the $[Ti(H_2O)_6]^{3+}$ complex?

What is pairing energy $(P)$? Explain the distribution of $d^n$ ($n=1$ to $10$) electrons in high spin and low spin octahedral complexes.

$\left[ Ti \left( H_{2} O \right)_{6} \right]^{3+}$ absorbs light of wavelength $498 \, nm$ during a $d-d$ transition. The octahedral splitting energy for the above complex is $....... \times 10^{-19} \, J$. (Round off to the Nearest Integer). Given: $h = 6.626 \times 10^{-34} \, Js$,$c = 3 \times 10^{8} \, ms^{-1}$.

Which of the following cannot be explained by crystal field theory?

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