Dative bond confusion (or coordinate bond)

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SUMMARY

The discussion clarifies the concept of dative bonds, particularly in the context of complex ions like Cu2+. When NH3 donates a lone pair to H+, it stabilizes the ion, while in Cu2+ complexes, lone pairs from water molecules are donated to the d-orbitals of copper, leading to hybridization. This hybridization results in a trigonal bipyramidal geometry when five ligands are present, but with six water molecules, a different structure is adopted. The conversation emphasizes the importance of understanding hybridization and ligand types in complex formation.

PREREQUISITES
  • Understanding of dative bonds and their role in coordination chemistry.
  • Familiarity with hybridization concepts, specifically dsp3 hybridization.
  • Knowledge of complex ion formation and ligand types.
  • Basic principles of molecular geometry and orbital theory.
NEXT STEPS
  • Research Werner's theory of coordination complexes.
  • Study the hybridization process in transition metal complexes.
  • Explore the geometry of coordination compounds, focusing on trigonal bipyramidal and octahedral structures.
  • Investigate Tollen's reagent and its applications in organic chemistry.
USEFUL FOR

Chemistry students, educators, and professionals in the field of coordination chemistry seeking to deepen their understanding of dative bonds and complex ion structures.

dilan
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I am a little confused with this. I know what a dative bond is, but the problem is when it comes to complex ions I do not understand.

ok now for example

NH_3 + H^+ = NH_4^+

So in this the lone pair of NH3 will fill the s- subshell of H and make it stable,

but say in Cu^2^+
when this attracts six water molecules with six lone pairs, where do these lone pairs go? I mean what subshell does it fill?I really appreciate if you can help me with this.
Thanks a lot
 
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they are dumped into the LUMO.
 
They go into a higher energy orbital.

Its more advanced than it seems though, The different shells actually sort of combine in a way called hybridisation, these shells form a difinitive shape. The lone pairs partially go into these hybridisation shells.

i think someone else could probably describe it more correctly. I'm not too confidant on the subject myself.
 
When cu2+ is hydrated, the lone pairs of electrons present on the oxygen atom of water are 'donated' to the d-orbital of the copper 2+ ion. This is why copper can form complexes (thats what the species is called).

This species has a certain structure which depends on the type of ligand attacking (in this case water), the number of bonds formed, and where the lone pairs go. Here, the orbitals undergo dsp^3 hybridisation (that basically means the number of lone pairs present in the respective orbital: in this case, 1 in 3d, 1 in 4s, and 3 in 4p) to give the species trigonal bipyramidal geometry (a triangle with two bonds perpendicular to the plane sticking out of the center).

Look up werner's theory/ability of d-block metals to form complexes if you want more detail.

Another example of a complex is Tollen's reagent [Ag(NH3)4]+ which gives your famous silver mirror test for aldehydes.
 
If the copper is hydrated with 6 molecules of water, it cannot adopt a trigonal bipyramid structure. Only 5 ligands are required for a trigonalbipyramid...
 

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