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May 22, 2009

Happy Anniversary!

Filed under: Photography, Outdoor Adventures, Chemistry, Music, Random, Life Outside of Lab - Administrator @ 10:34 am

 Today marks my Two-Year Anniversary in Colorado.  (You can read about Year One here).  It has been an eventful year, but instead of writing about it I’m going to let the pictures tell the story.  Coincidentally, I purchased my first dSLR almost a year ago (and my second today!), so there were quite a few pictures to go through.

As soon my D1x arrived, I peeled out of the driveway with Jeff and caught the sunset at Pawnee Buttes.

Finally, a gas grill.  It has changed my life.

 First camping trip of the year in RMNP.

I went home for the River Festival, built my stage, and came back the next day to this.  I miss thunderstorms.

Moonrise as seen from Horsetooth Rock.  Too bad there were too many clouds to see the moon.

 

 The first picture pretty much sums up our trip to the Great Sand Dunes.

 Ryan and I thought that it would be dry enough to backpack the Rawah Trail in July.  Wrong.

Jenni, Aaron and I climbed Castle and Conundrum Peaks.  And glissaded down.

 Backpacking Take II.  Success.  Along with summits of Chiquita and Ypsilon.

 

Mile High Music Festival brought these two together in my living room.  Now they’re married.

 

Kelso Ridge to Torrey’s.  Epic.

 

First trad climb in Gregory Amphitheatre, followed by Standard East Face of the Third Flatiron.

 

 Watched a triathlon and a bet-gone-wrong.  Yikes.  Still have those tan lines Aaron?

 420’s and bouldering at Independence Pass.

 

 Joe’s Valley.

 

 Fall trip to Boston to see Joe, then bouldering with Aaron in Lincoln Woods.

 About this time I became obsessed with off-camera lighting.  My first big project was a CFL.

 

 We met Aaron and Dan in California for a weekend of bouldering in Bishop.

 

 After Christmas, I climbed my first pitch of ice.

 

I took a few days off to check out the X-Games in Aspen…

…and then had the best powder day EVER at Steamboat.

 A new light bulb made an appearance with my bamboo.

Jeff and I launched carbonartphoto.com.


 In Ouray, I was lowered into a 135′ canyon with 2 ice axes.

 Deadpoint Magazine published one of my photos from Lincoln Woods.

 

I passed my 5th cume.


 In April I finally broke down and pieced together a rack…and then took pictures of it.

 

 Jeff and I shot our first wedding of the season.

 

 Spring climbing.

 

 Then Felix came for a visit…

…and the next week I passed my orals.

 

So ends another spectacular year in Colorado.

April 29, 2009

Facebook Ads

Filed under: Chemistry - Administrator @ 10:11 pm

 Acros, you don’t belong on facebook.  How dare you assume that I waste time at work on my computer surfing facebook.  However, I was just informed that we once again have money, so I think I might order some LDA and N-Boc-tryptophan-OMe from you.  And DMF.  Someone keeps breaking the bulb on our solvent system.

 

March 24, 2009

New Stool

Filed under: Rants, Chemistry, Random - Administrator @ 9:12 am

 I got a new stool today.  Really it is just my old chair.  The question now is do I (a) keep the stool, (b) find a new bolt, or (3) charge a new chair to my A-card?


March 11, 2009

Name Reactions: Installment 2

Filed under: Chemistry, Random - Administrator @ 12:50 pm

 Last spring, I proposed a new series of name reactions that every graduate student should know.  I learned a new one last weekend that I call "The MacBook Dehydration Reaction".  The experimental follows:


 

  MacBook (2).  To a MacBook running Firefox ChemDraw operating at r.t., add hot water (340 mL, 18.9 mol) in one batch, directly over the keyboard.  Stare with mouth agape until screen goes black, then disconnect AC power and remove battery to afford worthless shiny white paperweight 1.  Drain water and blow compressed air over the keyboard and battery compartment.  Place 1 in a large ziploc bag containing drierite (100 g) and seal.  Allow to dry at r.t. over 60 hours.  Plug in AC power and press power button.  Call Apple Tech Support and follow their directions.  After determining that your battery is dead, a new one will arrive in 24 hours.  Install new battery to afford MacBook 2 as a white solid (2040 g, 100%).  MP: 189-690 *C.

September 10, 2008

Novel, Gas-phase Recrystallization

Filed under: Rants, Chemistry - Administrator @ 3:35 pm

 I used to laugh at my colleagues who would go out of their way to climb a floor or two up in another wing of the building to avoid using the bathroom at the end of the chemistry wing.  I argued that it was usually reasonably clean and didn’t smell too bad.  The return of the undergrad hordes has changed my opinion, however.  The following theory that I propose is by no means original.  I will however commit fraud and present it as my own, despite the fact that either Aaron or Brandon originally gave me the idea.

 The source of my theory is the men’s room at the end of the hallway.  It has 2 stalls, 2 urinals, 2 sinks, and a shower that I don’t think ever gets used.  It also has no ventilation.  Lately, I’ve been holding my breath upon entering.  It is my theory that the unventilated air is a great solvent for the stench of shit.  Think of it as supersaturated with gaseous shit.  This smells bad enough on it’s own, but as soon as one enters a stall and drops a deuce, that piece of shit drops a seed crystal into the air that causes all previous shits from the week to crash out of solution.  I get excited when this happens in my flask in the hood; it means that pure crystals of my compound are forming and I get out of running a column.  I don’t want to smell your purified shit smell, however, so I now go 2 minutes out of my way to avoid your seed crystals.

Before               /                After

July 29, 2008

Should I Feel Guilty for Using My Fume Hood?

Filed under: Rants, Chemistry - Administrator @ 11:27 am

 Penn & Teller ridiculed some of the bullshit behind the "Green Movement" in their latest episode of Bullshit!.  Here’s a quick preview:


 One of the biggest loads of crap that they discussed in the episode was the idea of Carbon Credits.  The idea is that we all inevitably emit CO2 into the atmosphere by driving our cars, eating food, and running the air conditioner.  Shit, my fume hood is on 24/7, consuming the same amount of electricity as a single-family home annually.  Talk about CO2 emissions.  Companies like AtmosClear think that I should feel guilty about this and purchase Carbon Credits from them.


 Using their Emissions Calculator, I emit 19 tons of CO2 a year, under the national average of 25 tons.  If you factor in my fume hood, I estimate an additional 10 tons per year, bringing my total to a whopping 29 tons.  In order to become carbon neutral and clear my guilty conscience, I should purchase $185 worth of carbon credits to offset my emissions.  I estimate that the chemistry building has around 100 fume hoods, and at 10 tons of CO2 per hood, plus the extra 2 tons of CO2 used in the form of dry ice by our lab, the chemistry department owes Earth about $5,000.  Wait a second, AtmosClear is pro big business.  How is it that buying CO2 in bulk is any cheaper?  Buying 100 tons in bulk offers a savings of over $1000!

 Where exactly does your carbon money go?  According to the AtmosClear website, it looks like most of it goes to Des Plaines Landfill, where methane gas given off by trash is trapped and used to power homes.  A great idea.  New Belgium Brewery does that too.  My point: AtmosClear has a great business strategy; prey on global warming fears and guilt consumers into paying money for living.  You don’t have to buy carbon credits for driving your car, or working at a fume hood.  I don’t feel guilty, and until someone can prove that global warming is real and caused by humans, I will continue to not feel guilty.  I drive my car as little as possible, keep my thermostat turned up in the summer, and lower my hood sash at night, not to save the earth, but to save money.  Watch the Bullshit! episode below for Penn & Teller’s opinion.




July 23, 2008

Guide for the Perplexed Organic Experimentalist

Filed under: Chemistry - Administrator @ 1:45 pm

 A group down the hall recently cleaned out their lab space and a number of free books appeared in the hallway.  I quickly snatched up a book published in 1978 entitled "Guide for the Perplexed Organic Experimentalist."  My admiration of chemists of the past has grown over the years.  It is easy to take for granted the NMR located 30 feet from my desk or the instrument facility downstairs to which I can submit a sample for MS and receive a spectra back in less than a day.  Not to mention the wonders of my computer, which I can use to quickly draw chemical structures, predict NMR shifts, process/print/and store NMR spectra, render accurate 3D models of my molecule, determine if a substrate that has never been synthesized in a lab will (theoretically) fit in the binding pocket of a protein, search published chemistry literature for a specific reaction (as long as no one else is trying to do the same), type and revise manuscript or report drafts, and email coworkers or colleagues and potentially receive speedy replies to my inquiries.  The list goes on…

Over the past month, I have been reading Loewenthal’s guide, noting his particularly witty or outdated remarks for this weblog entry.  I’m not writing to pick fun at the old ways of chemistry, but rather to spread my appreciation of modern practices.  All quotes are taken from Loewenthal, H.J.E. Guide for the Perplexed Organic Experimentalist, 1978, 1-174.  My commentary is in italics.  Loewenthal’s in bold. Enjoy.

Refrigerators and Cold Rooms.  These may malfunction, and catch fire or explode, at any time.  Really?  Good thing my hood is 2′ away from our freezer.

 

At least once a day while in the laboratory stop and ask yourself what you would do should an accident or fire occur at that moment: …Where is the nearest sand bucket?  Does it contain sand or cigarette butts?  Just checked.  Our sand bucket contains neither sand nor cigarette butts.

When the components [of a prep-TLC plate] are coloured in the visible region one is often tempted to preserve the plate for posterity as the dernier cri in post-impressionist painting (anyone wanting to go in for his seriously is advised to use crude products from an oxidation with dichlorodicyanoquinone).  Our million dollar idea, Jeff?  I think Carbon Art LLC needs to sell mine.

In many institutions the demand for cleaning tissue reaches alarming dimensions at which point it becomes clear that it is being used for purposes best described as non-scientific.  I now suggest a reasonable and far more economic alternative: toilet paper.  In principle, it is exactly the same.  You will soon get over the psychological block; and if the secretarial staff do not, so much the better.  Non-scientific?  But Bob told us not to pick our noses in lab.

…that part of any library which houses [Beilstein’s Handbuch] is the most frequented one and that area should be reserved for Chemical Abstracts readers only.  It should also go without saying that no volume of this work should ever leave that area and that its binding should receive special care.  I love interlibrary loan.  I haven’t been to the library in search of scientific literature in months.

 

There was a time when the abstract would refer directly to all new compounds made, their melting or boiling points and possibly other physical properties, and outline details of their preparation.  And at that time the actual papers were just as boring as the abstracts.

[When writing to the author of a publication], do not forget to check whether there has not been a change in address from that given in the article, lest you commit the unpardonable offence<sic> of not knowing that the man has moved to a more prestigious institution.  I hope his email address hasn’t changed.

On organizing your information:  ‘Having it at your fingertips’ is a figure of speech commonly used.  You can turn it into reality only in the form of a Card Index.  There should be a card for every topic, and there should be cross-referencing cards pointing in all feasible directions.  You should always have a supply of cards with you; envelopes or paper napkins get lost, mixed up or used for other purposes.  There is no need to use the customary stiff cards; slips of ordinary paper cut to appropriate size will do just as well…Your Card Index is an extension of your memory cells and as such should remain strictly your private domain.  As your stack accumulates your popularity as a source of information with your co-workers will grow, but-never ever lend out cards to anyone else.  Am I screwed if my computer password is written on a napkin

It is safe to assume that any author who has taken care that his work is reliable and reproducible will have taken equal pride in describing the work accurately, clearly and unambiguously.  For example, the word ‘treat’ (’the solution was treated with…’) is frequently a convenient term to use when the author has forgotten exactly how it was done.  Wait, I’ve used the word ‘treated’ before…

It has been reported that placing a sheet of aluminum between the stirring motor and reaction flask improves evenness of stirring…  I love my IKA stirrer/hot plate combo.  And I don’t even have to use foil to make it work.

 

Above all, their [a Dewar’s] protective metal enclosure makes magnetic stirring well-nigh impossible.  Did I mention that I love my IKA?  I don’t have to use foil AND it can stir through a Dewar.

Wooden boiling sticks (applicators) are quite out and should be thrown away or put to some quite different use.  If applicators have been ‘out’ since 1978, why the hell are my students still required to use them when boiling a solution?

In many laboratories [ensuring an inert reaction atmosphere] is tackled by an array of often colorful and sometimes grotesquely (not to say downright Rabelaisian) shaped rubber balloons at strategic positions.  This looks cheerful on slides, but one soon finds out that this approach has severe limitations.  My balloons are quite festive.  They look cheerful in person, too.  I have yet to discover any limitations worthy of the ’severe’ descriptor.

On rubber septa and syringes: Some people swear by their use.  Many others swear while using them.  Only the most expensive types of septa are made of an elastomer which is resistant both to chemical attack and to the results of repeated puncturing.  Also it is difficult to find septa in a sufficient range of sizes to fit various openings or even just to fit all standard joint openings in common use.  A quick walk down to the stockroom and I can outfit my hood with appropriate sized septa for all of my glassware, resistant to chemical attack AND repeated puncture.  I both swear by their use and swear while using them, but then again, I tend to swear a lot.

 

Dropwise addition from a syringe, except when using an expensive and space-consuming device, can never be as simple and accurate as from a burette.  In my opinion the use of a syringe can be justified only where volumes of less than 0.05 ml are involved.  Just did a dropwise addition from a 10 mL syringe yesterday.  It was simple enough.

[Removal of grease from joints] is best done by wiping them several times with a tissue paper lightly soaked in a solvent such as carbon tetrachloride.  Carbon tetrachloride is scary shit.  Stick to hexanes.

On packing a column: In all cases the column should be perfectly vertical and should be vibrated by hand or with an electrical vibrator until the adsorbent has completely settled.  You keep a vibrator in the lab?

On TLC: How did we ever manage without it?  On the question of whether to make your own plates or to invest in the commercially available ones it is hard to give any definite advice.  How did we ever manage without commercially available TLC plates?

[Spotting TLCs] should always be done as uniformly as possible and reliance on home-made capillaries is not recommended.  Hey, my capillaries are home-made.  I’m damn proud of them too.

There is no sense recording [Rf values] unless with reference to a standard substance run on the same plate and at the same time [under the same atmospheric conditions].  Unless you are working in a laboratory which has automatic air conditioning these are entirely beyond your control.  I have air conditioning and I still see no sense in recording an Rf value.

It was said of Adolf von Baeyer that his success [in recrystallization] was in large measure due to his large beard harbouring seeds of every compound ever made.  However, even if beards are in fashion again this alone is not a good enough reason for following his example.  Some people believe in mascots or singing operatic arias; at least it cannot do any harm.  I need a mascot for my recrystallizations.  Suggestions?

 

Should you come across an ancient sewing machine, of the foot-operated type, requisition it.  The treadle, when connected to an electric motor, is a very suitable support for items to be shaken, and the open lattice work usually encountered makes firm attachment by springs or rubber bands an easy matter.  Talk about space-consuming.  Geesh.  Just use the sonicator.  It doesn’t require the use of springs and rubber bands to work.

A good tool for cutting [small filter paper circles] out of larger sizes is a very sharp and scrupulously clean cork borer with the appropriate diameter.  I wonder if the stockroom sells cork borers.  Wait, they sell every size of filter paper I could ever conceive using.

That’s all for now.  I doubt Loewenthal realized that he was writing a comedy for the 21st century.  Let it be known that I love my IKA stirrer, teflon stir bars, rubber septa, commercial TLC plates, argon balloons, the stockroom, and my computer.  In all fairness, I should also note that this book contained good suggestions that are still relavent to the modern perplexed organic experimentalist.  Not THAT much has changed.  This book is available for checkout on my desk…just don’t steal my giant stack of notecards.

May 10, 2008

Examples of Fine Lab Reports

Filed under: Rants, Chemistry - Administrator @ 11:42 pm

 Ah, students and their clever lab reports.  I took pictures while I graded today to document some of their fine work.  The first is an example of ambiguity:

 

 The, "throw in big words that we haven’t used yet in our conclusion in this sentence fragment" report:


 "I don’t want to look up any real safety info so we’ll make some up":

 

 

 "Hey, let’s blame the TA for our shitty yield!":

 

 One of my personal favorites, the concerted reaction mechanism:

 

 This conclusion is a little too concise:

 

 And this one is a little too long (this comment refers back to a statement made 3 pages earlier in the conclusion):

 

 ’A’ for effort doesn’t always apply.  I think "good try" is more appropriate:

 

 The complete NMR interpretation:

 

 The 40 page lab report: 

 

 I am now officially done grading lab reports for the semester.  The above examples are from one set of reports…as you can imagine, I’m glad to be done. 

May 5, 2008

ChemDraw Shortcuts

Filed under: Chemistry - Administrator @ 5:05 pm

 I’m lazy.  Maybe efficient is a better word.  Especially when working on the computer, I despise repetitive actions.  I will go out of my way to write a macro, create a shortcut, or use a hot key to avoid one extra keystroke.  Seeing as how creating schemes in ChemDraw is by nature a repetitive process, I feel that I have developed optimal drawing technique for minimizing keystrokes.  Use the following suggestions and cut 2 days off of your graduate school career.  Or take an extra coffee break per week.  I really don’t care how you use the extra time, but my 15 steps to ChemDraw success will make you happier, lose weight, and feel great about yourself.

 I’ll start out simple.  Draw a benzene ring.  Double click it.  Type ‘ctrl+c’ (or ‘apple+c’ for the mac toting readers).  Type ‘ctrl+v’.  Now you have 2 benzene rings!  Copy and paste will be your best friend when using ChemDraw.  You can highlight a structure to select it, but my experience has found double clicking an atom in the structure to be more reliable at selecting every atom.

 

 Simple.  Just wait.  It gets better.  Let’s turn benzene into pyridine.  How would you normally do that?  Probably by selecting the ‘Text’ tool, clicking one of the carbons on benzene, typing the letter N, and clicking off the molecule.  I can reduce that process to one step.  With the ‘Benzene’ tool still active, hover over one of the carbon atoms and type ‘n’.  Now you have pyridine.

 

 Now, how would you normally change that to piperidine?  Redraw the whole structure?  It is probably just as much work, but I’ll use this as an example for changing bond order.  Hover your mouse over one of the double bonds and type ‘1′.  Whoa.  It’s a single bond now.  Do that 2 more times and you’ve made piperidine!  You can change any bond to single, double, or triple in the same manner by typing 1, 2, or 3, respectively.

      

 Now, piperidine to 2-tert-butylpiperidine.  Select the ’solid bond’ tool, click the 2 position, then hover over the end of the new bond.  Type ‘8′ to "sprout" the 3 bonds of the t-butyl group.

      

 Now, define the stereochemistry of our new stereocenter.  To make this bond hashed, I used to delete the bond, pick the hashed bond tool, and draw in the new bond.  Turns out you can simply hover over the bond and type ‘h’ to make (S)-2-tert-butylpiperidine.

      

 Now, to demonstrate the next trick, I converted this to the chair form.  Notice the bond to the axial hydrogen in the structure below.  It should be solid, and the back C-C bond broken to show that it is behind the C-H bond.  To bring the C-H bond to the front, hover over the bond and type ‘f’.

 Charges can be added in the same way.  Hover over an atom and type ‘+’ or ‘-’.  That’s it for my cool hotkey tricks.  The next few suggestions are more commonly known, I think.  To align your structures so they are centered vertically with respect to the reaction arrow, select the products, reactants, and arrow, then right click > align > T/B centers. 

 

 For those of you studying name reactions, that is an Aza-Claisen Rearrangement.  I am usually very picky about alignment with my schemes, and I’ve found that an even quicker way of lining up reaction arrows and structures is to make use of the drawing grid.  It can be turned on or off using ‘ctrl+h’.  Arrows in my schemes are always the same length…this is a personal preference that most people don’t share with me.

 I also wanted to point out the character map toolbar in ChemDraw.  Any symbol not on the keyboard is on that toolbar.  To pull it up, click view > ‘Show Character Map Window’.

 

 The ‘clean-up structures’ tool (ctrl+shift+k) is good at fixing bond lengths and angles.  ChemDraw can also predict carbon and proton NMR spectra for molecules (Structure > Predict NMR Shifts).  Lastly, when typing in a formula, press ctrl+f to get ChemDraw to recognize it as a formula and sub-superscript appropriate numbers and charges.  That’s it for my tricks.  If you know more, please, enlighten me.

 All of the structures above were drawn with my favorite object settings (very similar to the ACS Document 1996 preset).

 

 Happy ChemDrawing.  I expect $5 for every new trick I taught you. 

April 28, 2008

Name Reactions

Filed under: Chemistry - Administrator @ 8:53 pm

I’m tired of studying name reactions.  The following five reactions were optimized and named by me (except for the 1st one, which I received on a postcard from New Belgium Brewery):

 (a) The Poultrification Reaction (best yields are obtained on Sunday afternoon)

 

 (2) Ethanol-catalyzed Degradation of the Over-worked and Underpaid Graduate Student


(question: does the amount of a reagent need to exceed 100 mol % before considering it stoichiometric as opposed to catalytic?)

 (3) The Houseplant Dehydration Reaction

 

 (b) The Payday Reaction (best yields obtained on 1st day of the month)

 

 (e) Four-Component Lab Report Elimination Reaction 


Back to work.  I’m pretty sure the other 229 reactions that I should learn are more likely to be on the exam. 

Safety Showers

Filed under: Chemistry, Random - Administrator @ 2:25 pm

 I just got another "Jam at Registration Roller" error…I’ve been watching Criminal Minds this weekend, and they always look for the stressor in an unsub’s life that makes them go serial.  I think I know what my stressor is, and I’ve resorted to serial blogging.  Anyway, we had a discussion at lunch today about a student using the safety shower for a "chemical" spill.  The guy broke a test tube containing 2 mL of water, 3 drops of 0.1 M nitric acid, and a small amount of an ionic compound.  He got a little on his hand (and hair?), freaked out, and pulled the safety shower.  I know that you should be better safe than sorry, but honestly, they don’t let general chemistry students near anything that requires a safety shower.

 I am a little jealous though, as I have yet to see a safety shower in operation.  I test the emergency eye wash station in my lab at least daily and I’ve had water fights in Brian’s lab with the safety drench hose, but I’ve never had the balls to pull the shower lever.  I’m thinking about talking one of my students into pulling it tomorrow…we’ll see how that goes.  I did find a decent video (with some really obnoxious guys in it) of a safety shower, which I’ve included below:


  I still want to see one go off in person, but this will do for now.

 UPDATE: Why does the teacher tell the student to take his shoes off in a chemistry lab?  She may have to demonstrate the first aid kit next.

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