Showing posts with label base. Show all posts
Showing posts with label base. Show all posts

Monday, January 11, 2010

Maze Solving by Chemotactic Droplets


a very interesting paper.
in jacs asap.

Solving maze problems is not only relevant to the everyday issues
of urban transportation1 and to experimental psychology2 but is
also one of the model problems of network and graph theory3 as
well as robotics.4 With the advent of computers, algorithms for
maze solving have become automated, but the solution times still
scale unfavorably with maze size/complexity.5 Several groups have
thus explored the possibility of maze solving by physical, chemical,
or even biological systems: microfluidic networks,6 chemical waves7
or plasmas,8 or microorganisms growing in response to food
gradients within the maze.9 Inspired by the latter example, we
wished to create a system in which an inanimate/chemical construct
would be self-propelled and solve mazes in response to chemical
stimuli. Here we describe one such system comprising small
droplets powered by the combination of acid/base chemistry and
surface tension effects. When subject to a pH gradient within a
maze, these droplets move toward regions of low pH and find the
shortest of multiple possible paths. Taxis in our system is over
distances of several centimeters and derives from the convection
flows developed outside of the droplets.1

Friday, January 16, 2009

Titrating n-buLi,s-buli, t-buli

method 1:

Take a briquette of menthol (usually about 80-100 mg), dissolve that in dry THF (~2 mL) and then add 1-2 mg (you don't need to really weight it) of triphenylmethane. You can roughly calculate how much of your lithium reagent you will need, and then add it dropwise to the solution of menthol/Ph3CH/THF. When all the menthol is deprotonated the triphenylmethane will be deprotonated abnd the solution will turn pink (eventually dark red if you add to much), then you can back calculate the concentration based on the volume of alkyl lithium you added. I usally carry this procedure out in triplicate ad average the results. It really only takes about 30 mins start to finish and it doesn't take much material either.

note:
1,1'-dipyridyl can also be used instead of triphenylmethane.




a link:
http://www.chemistry.mcmaster.ca/emslie/Titrating%20Alkyllithium%20Reagents%202.pdf

Thursday, December 11, 2008

KHMDS is nucleophilic ??



In this rxn, the base KHMDS removed the benzoyl group! at -20C.
I guess the bulky silane attacked the ester and the alcohol was freed.
so the conclusion is KHMDS is quite nucleophilic.