Anyone know where I can get a manual for:
Optomechanics Research model 10C Grating Spectrograph (Astronomical)
A photocopy or computer scan of it would be fine.
Thanks: Ed
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Dear Colleagues,
On behalf of the HEN 2008 Organizing Committee, I would like to
invite you to the 7th International Conference " Human Ecology and
Nature" (HEN 2008), which will be held in Moscow and Ples, Russia,
June 27-July 2, 2008.
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Sincerely,
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Announcement
& Call for Papers
STATE UNITARY FIRM MOSCOW SCIENTIFIC
AND INDUSTRIAL ASSOCIATION "RADON"
Organize the 7th International Conference
"HUMAN ECOLOGY AND NATURE" , Moscow-Ples, Russia, June 27-July 2,
2008.
In 1998, the 1st International Scientific Conference "Human ecology
and nature" has been organized jointly by the Ivanovo State
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the results of the Conference, the program and the conference
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According to the accepted decision, in 1999 the All-Russian
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Organization committee welcomes the participation in the Conference
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students.
The purposes of the International Conference "Human ecology and
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- Sergey A. Dmitriev (Chairman) Dr.Sc., Prof., Russia;
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Academician of RAAS, Russia;
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India;
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Russia;
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ORGANIZING COMMITTEE
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-
SCIENTIFIC PROGRAM: TOPICS
Symposium I "General ecology»
Chairpersons:
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Russia;
Symposium II "Molecular chemistry, physics and biology of
heterogeneous systems in ecology"
Chairpersons:
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Symposium III "Information problems of ecology"
Chairpersons:
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- Andrei I. Sobolev, Dr.Sc., Prof., Russia
Symposium IV "Radiobiology and Radioecology"
Chairpersons:
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ANDREW M. YAKOVLEV
Crystallography Institute of RAS, Moscow
HENRY S. MORGAN, ZEYNEB ZAAHAN
Casablanca State University, Casablanca, Marocco
E-mail: human-ecology@...
ELECTRICAL PROPERTIES OF ZnP2 SINGLE CRYSTALS OF TETRAGONAL AND
MONOCLINIC MODIFICATIONS
Measurements are made of the electrical properties of both
modifications of ZnP2 crystals, which are doped, undoped and annealed
vacuum and in vapor of the components. The measurements are carried
out in the temperature range from 190 to 380K. The donor centers7 are
found to be vacancies of phosphor. The dominating scattering
mechanism [1]............ ...
References:
1. Clark N.A. // Mol. Cryst. Lig. 1983. V. 94. # 1. P. 130.
REGISTRATION AND PARTICIPATION
Participants are requested to submit their papers accompanied by the
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STATE UNITARY FIRM MOSCOW SCIENTIFIC
AND INDUSTRIAL ASSOCIATION "RADON"
organize
the 7th International Conference
"HUMAN ECOLOGY AND NATURE"
Moscow-Ples
Russia
June 27-July 2, 2008.
1. Full name,
2. Rank and title,
3. The both home and affiliation addresses, phones and
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to the organizing committee via post or e-mail
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Address of the organizing committee:
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Participants will be hosted in hotels with maximum price up to 150
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Presentations:
Time of an oral presentation is 10-15 minutes. Presentation should
include: task; methods; main body (basic results) and conclusion.
Overhead projector will be available at the conference.
Official languages of the Conference are
Russian and English.
> Hello,
> I'm an amateur scientist in Denver, CO, looking to expand my lab a
> bit. I would like to be able identify different compounds in a
> solution of (whatever), and have a computer identify the ingredients.
>
> I *assume* I need:
> 1) a spectrophotometer with a computer interface and software
> 2) a way to seperate the individual compounds using chromatography
> (HPLC?)
> 3) a database to identify the individual spectra
> 4) I'm not sure what the most useful spectra are - IR / Vis / UV?
> 5) Are there any free computerized databases out there?
>
> This is brand new territory for me. What used system, which I might
> find on Ebay would be the best 'bang for the buck'?
>
> Thanks for your advice!
> Best regards,
> -Mark
I solve this problem using thin-layer chromatography combined with an old
grating IR instrument.
I can think of these advantages in this approach:
1) The chromatography is cheap and easy requiring very little equipment:
- Jars
- Solvents (certainly much less than HPLC)
- UV lamp
- Visualizing agents
2) You can find references for Rf values, developing systems, and
visualizing agents.
(It certainly helps if you know what your looking for.) TLC plates
show up on
Ebay all the time.
3) It's possible to make TLC semi-quantitative using some sort of
densitometry
....for example a computer scanner and freeware software such as Scion
Image.
(In the process, you'll learn a bit of image analysis.)
It's also possible to pick up instruments designed for TLC scanning on Ebay.
e.g.
http://cgi.ebay.com/ws/eBayISAPI.dll?ViewItem&category=26230&item=7503575157&rd=\
1&ssPageName=WDVWhttp://cgi.ebay.com/ws/eBayISAPI.dll?ViewItem&category=26230&item=7503599058&rd=\
1
4) You can do preprative TLC or column chromatography to isolate compounds.
From these isolations, you can then collect other important characterization
data such
as melting points etc.
You can do centrifugal TLC for preprative work using an instrument such as
this:
http://cgi.ebay.com/ws/eBayISAPI.dll?ViewItem&category=48720&item=7503488286&rd=\
1&ssPageName=WDVW
Be careful when buying any IR or UV spectrophotometer. I would certainly
try and
accertain whether the source works in any IR or UV instrument or UV HPLC
detector as
the replacement of them can be very costly.....if you can find the lamp.
You can get single wavelength detectors for HPLC pretty cheap but again,
make sure the UV source works.
A simple HPLC pump and injector can certainly be put together. If you run
in isocratic
mode you could recycle the mobile phase easily. The chromatography will be
less versatile (powerful).
Software for matching UV/VIS spectra exists but there's some significant
limitation in what you can identify from a UV/VIS
spectrum. Any molecule with a particular chromophore(s) is going to give
essentially the same UV/VIS spectrum.
Outside mass spec, I tend to think IR spectroscopy gives you the largest
information content concerning unknown
identification. It's possible to build your own IR libraries and code the
software to do library searches, but it would be
a big project. It's probably better just to use your head and 'interprete'
the IR spectra. Of course getting a good
IR spectrum depends on your success in isolation of compounds via TLC etc.
What you're wishing for in terms of having an instrument identify all the
unknowns in a mixture is probably best met by a
GC/MS, but what are the chances of actually coming up with such an
instrument via Ebay cheaply? I think slim.
My advice is to consider TLC and a good dose of "old school" organic
chemistry thinking. Do some research
into the techniques of the organic experiementalists before the advent of
modern computerized instrumentation.
Take to heart these words by Albert Hoffman:
"For structure determination, which today can be conducted rapidly and
elegantly with the help of spectroscopic
methods (UV, IR, NMR) and X-ray crystallography, we had to rely, in the
first fundamental ergot studies,
entirely on the old laborious methods of chemical degradation and
derivatization."
LSD, My Problem Child p.10
"PhotochemCAD is a computer-aided research and teaching tool for the field of photochemistry. PhotochemCAD contains a master molecule database of absorption and fluorescence spectra of 150 compounds, including molar absorption coefficients (e), fluorescence quantum yields (), and original literature references for almost all compounds. Molecular structures are displayed upon viewing the spectra. A database of solar spectra also is included. Modules are available for performing a variety of calculations that use absorption and fluorescence data, including calculation of oscillator strength, transition dipole moments, natural radiative lifetimes, and Fφrster energy-transfer rates and yields. Other modules enable multicomponent analysis calculations, simulations of fluorescence spectra upon energy transfer among linear arrays of pigments, calculations of blackbody radiator curves, and display of Gaussian, Lorentzian and/or delta functions. The spectra can be displayed on various scales (l in nm, n in Hz or , etc.), and manipulated in various ways. The compounds in the database are predominantly organic in nature with an emphasis on those that are biologically relevant and those with absorption in the visible region of the spectrum. The compound classes are shown in the following table along with one representative member of each class. The number of spectra refers to absorption spectra. The number of spectral sets (absorption and fluorescence) exceeds the number of compounds because several compounds have been examined in more than one solvent."
Hello, I'm an amateur scientist in Denver, CO, looking to expand my lab a bit. I would like to be able identify different compounds in a solution of (whatever), and have a computer identify the ingredients.
I *assume* I need: 1) a spectrophotometer with a computer interface and software 2) a way to seperate the individual compounds using chromatography (HPLC?) 3) a database to identify the individual spectra 4) I'm not sure what the most useful spectra are - IR / Vis / UV? 5) Are there any free computerized databases out there?
This is brand new territory for me. What used system, which I might find on Ebay would be the best 'bang for the buck'?
Frankly Mark, the best advice that I can give you is to go study chemistry for a while first. (however you go about that.)
Bill
In a message dated 4/5/05 12:42:08 PM Pacific Daylight Time, mark@... writes:
Hello,
I'm an amateur scientist in Denver, CO, looking to expand my lab a
bit. I would like to be able identify different compounds in a
solution of (whatever), and have a computer identify the ingredients.
I *assume* I need:
1) a spectrophotometer with a computer interface and software
2) a way to seperate the individual compounds using chromatography
(HPLC?)
3) a database to identify the individual spectra
4) I'm not sure what the most useful spectra are - IR / Vis / UV?
5) Are there any free computerized databases out there?
This is brand new territory for me. What used system, which I might
find on Ebay would be the best 'bang for the buck'?
Hello,
I'm an amateur scientist in Denver, CO, looking to expand my lab a
bit. I would like to be able identify different compounds in a
solution of (whatever), and have a computer identify the ingredients.
I *assume* I need:
1) a spectrophotometer with a computer interface and software
2) a way to seperate the individual compounds using chromatography
(HPLC?)
3) a database to identify the individual spectra
4) I'm not sure what the most useful spectra are - IR / Vis / UV?
5) Are there any free computerized databases out there?
This is brand new territory for me. What used system, which I might
find on Ebay would be the best 'bang for the buck'?
Thanks for your advice!
Best regards,
-Mark
Hi,
Yes, it depends on wavelength.
Actually it is described for visible region. This is of your interest.
Regards,
Vandana
On Mon, 4 Apr 2005, talkme wrote:
> Hii Everybody
>
> can any one tell me if i use
> Microscope's microobjctive (MO) to focus a laser
> beam,does it focus exactly according to its
> magnification number?
>
> i tell it different way,if i use He-Ne ~ 100 micron
> spot to focus with 50X MO,will it make the spot size 2
> micron in focal plane ?? is it wavelength
> dependent,like IR,VIS,UV..i am interested in VIS only.
>
> thanks in advance
>
> regards
> Dinesh
>
>
>
> #####################################################
>
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> there."
>
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>
>
>
>
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>
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Hii Everybody
can any one tell me if i use
Microscope's microobjctive (MO) to focus a laser
beam,does it focus exactly according to its
magnification number?
i tell it different way,if i use He-Ne ~ 100 micron
spot to focus with 50X MO,will it make the spot size 2
micron in focal plane ?? is it wavelength
dependent,like IR,VIS,UV..i am interested in VIS only.
thanks in advance
regards
Dinesh
#####################################################
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Read only the mail you want - Yahoo! Mail SpamGuard.
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Well you know how it is that once there is an interesting looking problem that should have a simple solution, there is nothing you can do about the tendency to keep thinking about it as you are reading and so forth. vandanas@... asked how to make C2H5OD. Here is a solution that ought to be easy to do:
Take pure anhydrous ethanol, it must be anhydrous or it will not work, and add metallic sodium to it. You will get the salt C2H5ONa from this and hydrogen gas evolves. Bubbles of H2 will tell you that the reaction is proceeding and you have the sodium alcoholate. If you now add ordinary water the salt will hydrolyze to ethanol + NaOH. That much is known but do not do that. If instead of water, you add an excess of D2O you should get your C2H5OD and NaOD. I did not look up the
dissociation constants of D2O -> D+ + OD-
and of C2H5OD -> D+ + C2H5O-
but D in the alcohol should be much smaller than D in the D2O for this to work. This would be true for the case of hydrogen, so it should be true for deuterium, too.
Bill Isakson
-----William E.J. Isakson, El Cerrito, CA, CatalyticChemist@...
http://members.aol.com/WeAlsoWalk We Also Walk
American Chemical Society member
American Institute of Chemical Engineers member
American Radio Relay League member
Society for the History of Alchemy and Chemistry member
Oh! I thought you wanted all the H's to be D's. If it is just the hydroxyl D that you want, just start with an alkyl halide and either treat it by heating with NaOD or KOD in D2O or even just do it in gas phase with D2O and R-X heated under some pressure. The analogous reactions for hydrogen, to make R-OH from R-X are well known, see any textbook. And again, when you finally do get product you can write this up and publish it. Then people can refer to your work and yhou will be in all the footnotes.
Bill
In a message dated 3/17/05 8:30:46 AM Pacific Standard Time, vandanas@... writes:
I didn't ask the process of denaturing. I wanted to know the procedure of
making deuterated ethanol (C2H5OD).
Hi Varathu,
I didn't ask the process of denaturing. I wanted to know the procedure of
making deuterated ethanol (C2H5OD).
Regards,
Vandana
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
Vandana Sharma
Laboratory Astrophysics,
LAB- 570
Space and Planetary Atmosphere Division,
Physical Research Laboratory,
Navrangpura,
Ahmedabad- 380 009
Gujarat, India
Phone No : (91)-079-26302129-Ext-4570/4567(lab)
Mobile:09426533036
Email : vandanas@...van_res@...
URL : http://www.prl.ernet.in/~vandanas
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
On Mon, 14 Mar 2005, varathu rajan wrote:
> Hi,
>
> I think a drop of metanol is enough to denature the etanol.
>
> urs
> Varatharajan.
>
> Vandana Sharma <vandanas@...> wrote:
>
>
> Hello all,
>
> Does any body know the method of making Deuterated Ethanol?
>
> Expecting reply.
>
> Vandana
>
> ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
> Vandana Sharma
> Laboratory Astrophysics,
> LAB- 570
> Space and Planetary Atmosphere Division,
> Physical Research Laboratory,
> Navrangpura,
> Ahmedabad- 380 009
> Gujarat, India
>
> Phone No : (91)-079-26302129-Ext-4570/4567(lab)
> Mobile:09426533036
> Email : vandanas@...
> van_res@...
> URL : http://www.prl.ernet.in/~vandanas
> ~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
>
>
>
>
>
>
>
>
> Yahoo! Groups Links
>
>
>
>
>
>
>
>
>
> ---------------------------------
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I am trying to figure out the reason why someone would want deuterated ethanol. Since deuterated ethanol is heavier, normal ethanol should be more useful.
Harris
CatalyticChemist@... wrote:
In a message dated 3/14/05 7:46:14 AM Pacific Standard Time, vandanas@... writes:
Hello all,
Does any body know the method of making Deuterated Ethanol?
Expecting reply.
Vandana
Well, I would go make a deuterated ethene and then add dueterated water across the double bond. The reactions for hydrogen are well known catalytic reactions. Substitute D for H and write up the differences. However, definitely proceed with caution with that because a couple of guys at my alma matre, SRI International, blew themselves and the whole room up playing with small quantities of Deuterium on catalysts. The they said it was cold fusion, but the establishment says that is impossible. Anyway they died and the room disappeared. Bill Isakson -----William
E.J. Isakson, El Cerrito, CA, CatalyticChemist@... http://members.aol.com/WeAlsoWalk We Also Walk American Chemical Society member American Institute of Chemical Engineers member American Radio Relay League member Society for the History of Alchemy and Chemistry member
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In a message dated 3/14/05 7:46:14 AM Pacific Standard Time, vandanas@... writes:
Hello all,
Does any body know the method of making Deuterated Ethanol?
Expecting reply.
Vandana
Well, I would go make a deuterated ethene and then add dueterated water across the double bond. The reactions for hydrogen are well known catalytic reactions. Substitute D for H and write up the differences. However, definitely proceed with caution with that because a couple of guys at my alma matre, SRI International, blew themselves and the whole room up playing with small quantities of Deuterium on catalysts. The they said it was cold fusion, but the establishment says that is impossible. Anyway they died and the room disappeared.
Bill Isakson
-----William E.J. Isakson, El Cerrito, CA, CatalyticChemist@...
http://members.aol.com/WeAlsoWalk We Also Walk
American Chemical Society member
American Institute of Chemical Engineers member
American Radio Relay League member
Society for the History of Alchemy and Chemistry member
Hello all,
Does any body know the method of making Deuterated Ethanol?
Expecting reply.
Vandana
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
Vandana Sharma
Laboratory Astrophysics,
LAB- 570
Space and Planetary Atmosphere Division,
Physical Research Laboratory,
Navrangpura,
Ahmedabad- 380 009
Gujarat, India
Phone No : (91)-079-26302129-Ext-4570/4567(lab)
Mobile:09426533036
Email : vandanas@...van_res@...
URL : http://www.prl.ernet.in/~vandanas
~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~~
If you have information about then could you please drop the site address of all in this "spectroscopic group's" mail box.
Looking forward to see your reply.
Kind regards, Vandana
Vandana Sharma Laboratory Astrophysics, LAB- 570 Space and Planetary Atmosphere Division, Physical Research Laboratory, Navrangpura, Ahmedabad- 380 009 Gujarat, India
> > hello everybody.i have some informstion and addresses of some good > site about group theory and it's application in specteroscopy.and > about symmetic moleculs and character table.thanks > > > > > Yahoo! Groups Sponsor > ADVERTISEMENT > click here > > ________________________________________________________________________________ > Yahoo! Groups Links > * To visit your group on the web, go to: > http://groups.yahoo.com/group/spectroscopy/ > > * To
unsubscribe from this group, send an email to: > spectroscopy-unsubscribe@yahoogroups.com > > * Your use of Yahoo! Groups is subject to the Yahoo! Terms of Service. > >
Hi Matin,
If you have information about then could you please drop the site
address of all in this "spectroscopic group's" mail box.
Looking forward to see your reply.
Kind regards,
Vandana
Vandana Sharma
Laboratory Astrophysics,
LAB- 570
Space and Planetary Atmosphere Division,
Physical Research Laboratory,
Navrangpura,
Ahmedabad- 380 009
Gujarat, India
Phone No : (91)-079-6302129-Ext-4570/4567(lab)
Email : vandanas@...van_res@...
URL : http://www.prl.ernet.in/~vandanas
On Fri, 12 Nov 2004, Matin wrote:
>
> hello everybody.i have some informstion and addresses of some good
> site about group theory and it's application in specteroscopy.and
> about symmetic moleculs and character table.thanks
>
>
>
>
> Yahoo! Groups Sponsor
> ADVERTISEMENT
> click here
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>
hello everybody.i have some informstion and addresses of some good
site about group theory and it's application in specteroscopy.and
about symmetic moleculs and character table.thanks
Hi. Have anybody been testing b-irradiated PMMA (low doses) using positron annihilation lifetime spectroscopy? My results show a unique peak (40%) of I2 and T2 at about 7 kBq. Irradiation was at air at r.t.
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Hello everyone
My name is William Goosen.
I am a Masters student at the University of Port Elizabeth in South
Africa.I am currently studying Raman spectroscopy at our Physics
department, focusing specifically on solid state thin films.
Hey,
I am a research student at polytechnic university and I have
combined Polyacrylonitrile with CNT's, and have taken an infrared
spectra of my composite film. Would anyone be able to help interpret
the spectra recieved and possible reasons for variations once the
spectras are compared?
Thanks!
Hi.
I am a master student in Turkey and my thesis is related to the
(e,2e) technique in obtaining information on both structure and
collision dynamics and the electron impact spectroscopy: from atom to
solids.
The possibility of investigating the electronic structure of solids
is largely based at present upon measurements of excitation energies
and transition probabilities. In spite of the large number of
spectroscopies currently used to characterize the electronic
structure of surfaces, none of them is capable of measuring momentum
distributions. Although it is very sensitive to fine details of the
wavefunction, the electron momentum density is not as widely
investigated as the other observables because ionization experiments
are needed to measure it, with completely determined kinematics.
Coincidence experiments of this kind, in particular (e,2e) and
coincidence Compton scattering experiments are the only available
spectroscopies capable of providing both binding energies and
momentum densities of the single particle states of the quantum
system under study.
The (e,2e) spectroscopy and the coincidence Compton scattering have
already shown their capability to investigate bulk properties of
solids. In particular, (e,2e) has already produced a fairly large
body of resuls on thin film momentum distributions. As far as
coincidence Compton experiments are concerned, it must be noted that
because of the smallnes of the cross section they are becoming
feasible and available for massive investigations only with the
advent of third-generation synchrotron sources. Their energy
resolution, however, is still not as goos as in the (e,2e)
experiments.
Best regards
Omer Sise
Department of Physics
Afyon Kocatepe University
Dear Varathu,
Rahul is right. Only if the molecule is assymetric (heteronuclear) will
rotational spectrum be observed, since if it is homonuclear there will be
no dipole component change during the rotation and hence no interaction
with radiation. But you can't understand what the selection rules and
dipole terms are until unless you have completed your first year M.Sc.
So here the anwer goes in a classical manner (not in QM al)
The basic requirement for the emission or absorption of radiation by a
transition between rotational energy states is that the molecule must have
a permanent dipole moment. This is what the classical electrodynamics
says. Accor. to this a rotating molecule can lead to emission of radiation
only if a changing dipole moment is associated with it. Heteronuclear
diatomic molecules with unlike atoms, for which the centers of +ive and
-ive charges don't coincide, hence have a dipole moment. During the
rotation of the molecule the component of the dipole moment in a fixed
direction changes periodically with the frequency of rotation,v , of the
molecule so that, classically, the radiation of frequency v should be
emmited. Homonuclear molecules have no dipole moment and hence there is no
emmision of IR radiation.
I think this answers your question.
Best wishes,
Vandana
Vandana Sharma
Laboratory Astrophysics,
LAB- 570
Space and Planetary Atmosphere Division,
Physical Research Laboratory,
Navrangpura,
Ahmedabad- 380 009
Gujarat, India
Phone No : (91)-079-6302129-Ext-4570/4567(lab)
Email : vandanas@...van_res@...
URL : http://www.prl.ernet.in/~vandanas
On Sat, 3 Jul 2004, [iso-8859-1] varathu rajan wrote:
> Dear Madam,
> My question is why a molecule should have permanent dipole moment to
absorb the Micro Wave radiation.
> In other words why molecules such as Hydrogen does not give rotational
spectra?
> Similarly why symmetrical stretching of CO2 is Infrred inactive?
>
> Friendly,
> Varathu.
>
> Vandana Sharma <vandanas@...> wrote:
> Dear Varathu,
>
> Could you please elaborate your question.
>
> Regards,
> Vandana
>
>
> Vandana Sharma
> Research Scholar
> Laboratory Astrophysics,
> LAB- 570
> Space and Planetary Atmosphere Division,
> Physical Research Laboratory,
> Navrangpura,
> Ahmedabad- 380 009
> Gujarat, India
>
> Phone No : (91)-079-6302129-Ext-4570/4567(lab)
> Email : vandanas@...
> van_res@...
> URL : http://www.prl.ernet.in/~vandanas
>
> On Thu, 24 Jun 2004, [iso-8859-1] varathu rajan wrote:
>
> > Dear Friends,
> >
> > I have a dobt in the fundamentals of spectrosopy.
> > My doubt is
> > 1.For a molecule to be MW active,why it should have permanent Dipole moment
&.
> > 2.To be IR active, why a molecule should undergo net change in its dipole
moment?
> >
> > Plz clear my doubts
> >
> > Friendly,
> > Varathu
> >
> >
> >
> > Yahoo! India Matrimony: Find your partner online.
>
>
>
>
>
>
> Yahoo! Groups Links
>
>
>
>
>
> Yahoo! India Careers: Over 50,000 jobsonline.
Hi Varathu,
There are lots of good books on spectroscopy which can give you a great
deal of information about the questions you are asking.
http://www.wiley.com/WileyCDA/WileyTitle/productCd-0471974218.html (High
Resolution Spectroscopy, Second Edition
J. Michael Hollas)
Anyway, it has do with the derivation of the selection rules for these
spectroscopies.
In IR, if you look at the basic eqaution of the transition moment
integral, we have dipole moment in it. This term is then expanded. After
applying the orthogonality theorem, one gets the selection rules for IR
which says that the dipole moment has to change along that coordinate. I
am sure you may not want to go into details unless and until you are
really after something. I guess the convention is to accept these
selection
rules (rules which define why we see some peaks in spectra and why not
other).
The answer for MW is also similar.
I hope Ms. Vandana will agree with this answer.
Thanks
- Rahul
Purdue University,
West Lafayette, IN 47907
*************************************************************************
On Sat, 3 Jul 2004, [iso-8859-1] varathu rajan wrote:
> Dear Madam,
> My question is why a molecule should have permanent dipole moment to
absorb the Micro Wave radiation.
> In other words why molecules such as Hydrogen does not give rotational
spectra?
> Similarly why symmetrical stretching of CO2 is Infrred inactive?
>
> Friendly,
> Varathu.
>
> Vandana Sharma <vandanas@...> wrote:
> Dear Varathu,
>
> Could you please elaborate your question.
>
> Regards,
> Vandana
>
>
> Vandana Sharma
> Research Scholar
> Laboratory Astrophysics,
> LAB- 570
> Space and Planetary Atmosphere Division,
> Physical Research Laboratory,
> Navrangpura,
> Ahmedabad- 380 009
> Gujarat, India
>
> Phone No : (91)-079-6302129-Ext-4570/4567(lab)
> Email : vandanas@...
> van_res@...
> URL : http://www.prl.ernet.in/~vandanas
>
> On Thu, 24 Jun 2004, [iso-8859-1] varathu rajan wrote:
>
> > Dear Friends,
> >
> > I have a dobt in the fundamentals of spectrosopy.
> > My doubt is
> > 1.For a molecule to be MW active,why it should have permanent Dipole moment
&.
> > 2.To be IR active, why a molecule should undergo net change in its dipole
moment?
> >
> > Plz clear my doubts
> >
> > Friendly,
> > Varathu
> >
> >
> >
> > Yahoo! India Matrimony: Find your partner online.
>
>
>
>
>
>
> Yahoo! Groups Links
>
>
>
>
>
> Yahoo! India Careers: Over 50,000 jobsonline.
My question is why a molecule should have permanent dipole moment to absorb the Micro Wave radiation.
In other words why molecules such as Hydrogen does not give rotational spectra?
Similarly why symmetrical stretching of CO2 is Infrred inactive?
Friendly,
Varathu.
Vandana Sharma <vandanas@...> wrote:
Dear Varathu,
Could you please elaborate your question.
Regards, Vandana
Vandana Sharma Research Scholar Laboratory Astrophysics, LAB- 570 Space and Planetary Atmosphere Division, Physical Research Laboratory, Navrangpura, Ahmedabad- 380 009 Gujarat, India
On Thu, 24 Jun 2004, [iso-8859-1] varathu rajan wrote:
> Dear Friends, > > I have a dobt in the fundamentals of spectrosopy. > My doubt is > 1.For a molecule to be MW active,why it should have permanent Dipole moment &. > 2.To be IR active, why a molecule should undergo net change in its dipole moment? > > Plz clear my doubts > > Friendly, >
Varathu > > > > Yahoo! India Matrimony: Find your partner online.
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