November 24, 2024, 02:58:36 AM
Forum Rules: Read This Before Posting


Topic: synthesis problem  (Read 4127 times)

0 Members and 1 Guest are viewing this topic.

Offline haichau

  • New Member
  • **
  • Posts: 3
  • Mole Snacks: +0/-0
synthesis problem
« on: July 28, 2009, 02:02:25 PM »
Can you explain why the wavelength increase when 4-aminothiophenol group substitute chlorine atom in heptamethine cyanide dyes ?
Example : ADS830WS has wavelength 819nm.When ADS830WS react with 4-aminothiophenol in DMSO ( a little NaOH added to mixture), the product ADS832WS has its wavelength 822nm (increase)_.Explain?
Thanks

Offline sjb

  • Global Moderator
  • Sr. Member
  • ***
  • Posts: 3653
  • Mole Snacks: +222/-42
  • Gender: Male
Re: synthesis problem
« Reply #1 on: July 28, 2009, 03:38:15 PM »
What happens in terms of the molecule when the amino group substitutes the chlorine, or when base acts on the thiophenol?

Offline haichau

  • New Member
  • **
  • Posts: 3
  • Mole Snacks: +0/-0
Re: synthesis problem
« Reply #2 on: July 29, 2009, 10:29:13 AM »
I have an experiment.The reactants are ADS830WS ( wavelength:819nm), NaOH, 4-aminothiophenol.After finish this experiment, I have product ADS832WS which have wavelength 824nm.The structure of ADS832WS have different which that of ADS830WS is chlorine atom at meso position have been replaced by 4-aminothiophenyl ( from 4-aminothiophenol).Help me this explain this ?

Offline sjb

  • Global Moderator
  • Sr. Member
  • ***
  • Posts: 3653
  • Mole Snacks: +222/-42
  • Gender: Male
Re: synthesis problem
« Reply #3 on: July 29, 2009, 03:06:07 PM »
Ahh, I misunderstood - do you now have 4-aminophenyl phenyl sulfide?

What is the nature of the electronic transition you're observing?

Offline haichau

  • New Member
  • **
  • Posts: 3
  • Mole Snacks: +0/-0
Re: synthesis problem
« Reply #4 on: July 30, 2009, 10:48:52 AM »
You can read this attachment obviously

Sponsored Links