September 28, 2024, 06:25:40 PM
Forum Rules: Read This Before Posting


Topic: complexes  (Read 3572 times)

0 Members and 1 Guest are viewing this topic.

Offline orgoclear

  • Full Member
  • ****
  • Posts: 176
  • Mole Snacks: +9/-13
complexes
« on: February 10, 2010, 12:04:27 AM »
Is hexaaquachromium(III) cation an inner orbital complex or an outer orbital complex. I have read somewhere that as the crystal field splitting energy of water is quite less, the lone pairs of O cannot be accommodated in the inner d-(vacant orbitals) consequently forming an outer orbital complex with hybridisation sp3d2 istead of the expected d2sp3. Is this correct?

Offline xoto

  • Regular Member
  • ***
  • Posts: 21
  • Mole Snacks: +0/-0
Re: complexes
« Reply #1 on: February 10, 2010, 03:48:13 AM »
look for m.gerloch, e.c constable. transition metal chemistry-the valence shell in d-block chemistry. i believe this book will be helpful

Offline orgoclear

  • Full Member
  • ****
  • Posts: 176
  • Mole Snacks: +9/-13
Re: complexes
« Reply #2 on: February 14, 2010, 04:49:43 AM »
can i have more views?

Offline renge ishyo

  • Chemist
  • Full Member
  • *
  • Posts: 403
  • Mole Snacks: +67/-14
Re: complexes
« Reply #3 on: February 15, 2010, 02:36:07 PM »
Well, I can only add that the [Co(H20)6]3+ ion is somewhat of a weirdo. It is the only first row transition metal that forms a low spin complex with the weak field H20 ligand (the other first row transition metals need a strong field ligand to form a low spin complex). Other than that, the book I used discouraged the use of hybrid orbitals when working with MO diagrams, so I am no help there  :-\

Sponsored Links