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	<title>Comments on: it takes some serious talent to screw this up</title>
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	<link>http://www.coronene.com/blog/?p=186</link>
	<description>A chemistry blog about organic materials, nanocrap, life in the lab and kittens</description>
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		<title>By: Aldrich still sells brown Tetrakis &#124; The Chem Blog</title>
		<link>http://www.coronene.com/blog/?p=186&#038;cpage=1#comment-8008</link>
		<dc:creator>Aldrich still sells brown Tetrakis &#124; The Chem Blog</dc:creator>
		<pubDate>Tue, 22 Sep 2009 22:18:59 +0000</pubDate>
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		<description>[...] Of course, you can make your own. [...]</description>
		<content:encoded><![CDATA[<p>[...] Of course, you can make your own. [...]</p>
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		<title>By: Carbon-Based Curiosities &#187; Blog Archive &#187; From A to Zinc Triflate</title>
		<link>http://www.coronene.com/blog/?p=186&#038;cpage=1#comment-3004</link>
		<dc:creator>Carbon-Based Curiosities &#187; Blog Archive &#187; From A to Zinc Triflate</dc:creator>
		<pubDate>Wed, 12 Mar 2008 03:12:30 +0000</pubDate>
		<guid isPermaLink="false">http://www.coronene.com/blog/?p=186#comment-3004</guid>
		<description>[...] We&#8217;ve talked about how tomake tetrakis yourself and it really is a super easy prep. But, as the saying goes, fuck it. You know what&#8217;s easier [...]</description>
		<content:encoded><![CDATA[<p>[...] We&#8217;ve talked about how tomake tetrakis yourself and it really is a super easy prep. But, as the saying goes, fuck it. You know what&#8217;s easier [...]</p>
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		<title>By: ComicBookChemist</title>
		<link>http://www.coronene.com/blog/?p=186&#038;cpage=1#comment-1780</link>
		<dc:creator>ComicBookChemist</dc:creator>
		<pubDate>Mon, 22 Oct 2007 22:30:00 +0000</pubDate>
		<guid isPermaLink="false">http://www.coronene.com/blog/?p=186#comment-1780</guid>
		<description>The secret to Jack&#039;s success is the love of Mien Troong.</description>
		<content:encoded><![CDATA[<p>The secret to Jack&#8217;s success is the love of Mien Troong.</p>
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		<title>By: David Eaton</title>
		<link>http://www.coronene.com/blog/?p=186&#038;cpage=1#comment-1730</link>
		<dc:creator>David Eaton</dc:creator>
		<pubDate>Fri, 12 Oct 2007 05:59:00 +0000</pubDate>
		<guid isPermaLink="false">http://www.coronene.com/blog/?p=186#comment-1730</guid>
		<description>Jack is fantastic. I think a lot of people don&#039;t get him, because he is so mild-mannered. But, right when you  get lulled into thinking he is above the fray, all of a sudden  he&#039;ll bust out some Zen Tai Chi of chemistry so profound it&#039;ll take weeks to absorb it. If you don&#039;t pay attention, it&#039;s gone.&lt;br/&gt; &lt;br/&gt;The guy seems to have a near photographic memory for the lit, too. I can&#039;t say enough good about Jack.</description>
		<content:encoded><![CDATA[<p>Jack is fantastic. I think a lot of people don&#8217;t get him, because he is so mild-mannered. But, right when you  get lulled into thinking he is above the fray, all of a sudden  he&#8217;ll bust out some Zen Tai Chi of chemistry so profound it&#8217;ll take weeks to absorb it. If you don&#8217;t pay attention, it&#8217;s gone.</p>
<p>The guy seems to have a near photographic memory for the lit, too. I can&#8217;t say enough good about Jack.</p>
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		<title>By: Ψ*Ψ</title>
		<link>http://www.coronene.com/blog/?p=186&#038;cpage=1#comment-1728</link>
		<dc:creator>Ψ*Ψ</dc:creator>
		<pubDate>Fri, 12 Oct 2007 03:15:00 +0000</pubDate>
		<guid isPermaLink="false">http://www.coronene.com/blog/?p=186#comment-1728</guid>
		<description>Ah.  He was my academic advisor before they changed the system around completely (which is too bad, because he&#039;s pretty much awesome).  Some of the projects he has (kinda) going right now are really cool, but there aren&#039;t enough people around to work on them.</description>
		<content:encoded><![CDATA[<p>Ah.  He was my academic advisor before they changed the system around completely (which is too bad, because he&#8217;s pretty much awesome).  Some of the projects he has (kinda) going right now are really cool, but there aren&#8217;t enough people around to work on them.</p>
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		<title>By: David Eaton</title>
		<link>http://www.coronene.com/blog/?p=186&#038;cpage=1#comment-1727</link>
		<dc:creator>David Eaton</dc:creator>
		<pubDate>Fri, 12 Oct 2007 03:06:00 +0000</pubDate>
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		<description>Yep. All he got out of me pub-wise was a weird Heterocycles paper on an unusual 10 membered ring that I made by accident. Too bad, because we had a quite a bit of steam going for a while.&lt;br/&gt;&lt;br/&gt;The ferrocene and manganese chemistry was working really well when Bossman walked up and said &quot;How would you like to try some acene chemistry.&quot; I figured he meant try something that one of the guys who recently graduated had abandoned. I figure it would crap out and the whole thing would die, because I figured the guys before me had beaten that stuff to death. Nope. I was constantly busy with something that was working well for the rest of the time I was in grad school. No complaints. Anything that gets you to escape velocity is fine with me. But I wish I had had another year or two. With a wife and son, that wasn&#039;t in the cards.&lt;br/&gt;&lt;br/&gt;Another guy in Jack&#039;s group picked up the Mn stuff, and now he&#039;s a prof at WKU.</description>
		<content:encoded><![CDATA[<p>Yep. All he got out of me pub-wise was a weird Heterocycles paper on an unusual 10 membered ring that I made by accident. Too bad, because we had a quite a bit of steam going for a while.</p>
<p>The ferrocene and manganese chemistry was working really well when Bossman walked up and said &#8220;How would you like to try some acene chemistry.&#8221; I figured he meant try something that one of the guys who recently graduated had abandoned. I figure it would crap out and the whole thing would die, because I figured the guys before me had beaten that stuff to death. Nope. I was constantly busy with something that was working well for the rest of the time I was in grad school. No complaints. Anything that gets you to escape velocity is fine with me. But I wish I had had another year or two. With a wife and son, that wasn&#8217;t in the cards.</p>
<p>Another guy in Jack&#8217;s group picked up the Mn stuff, and now he&#8217;s a prof at WKU.</p>
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		<title>By: Ψ*Ψ</title>
		<link>http://www.coronene.com/blog/?p=186&#038;cpage=1#comment-1726</link>
		<dc:creator>Ψ*Ψ</dc:creator>
		<pubDate>Fri, 12 Oct 2007 02:04:00 +0000</pubDate>
		<guid isPermaLink="false">http://www.coronene.com/blog/?p=186#comment-1726</guid>
		<description>Huh?  That&#039;s news to me, Dave...did you work for Selegue as well?</description>
		<content:encoded><![CDATA[<p>Huh?  That&#8217;s news to me, Dave&#8230;did you work for Selegue as well?</p>
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		<title>By: David Eaton</title>
		<link>http://www.coronene.com/blog/?p=186&#038;cpage=1#comment-1724</link>
		<dc:creator>David Eaton</dc:creator>
		<pubDate>Fri, 12 Oct 2007 01:27:00 +0000</pubDate>
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		<description>Excimer- I am also a huge fan of Ni(dppe)Cl2. It is cheap, and it is falling-off-a-log easy to make. &lt;br/&gt;&lt;br/&gt;I had the luxury in graduate school to work in two groups, one organic materials and one organometallic. Since my advisor was untenured at the time, I had to have a tenured co-advisor. I think in most cases at my alma mater, this is purely a formality, but my projects had enough overlap that I got to do some real organometallic work. &lt;br/&gt;&lt;br/&gt;The pentacene stuff killed off some really neat projects and brought my organometallic work to an abrupt halt. I made some really nifty 1,2 disubstituted ferrocenes, really cool compounds by 2 different and interesting routes, that never made it into print, which is one of my only regrets from grad school. There was not an obvious heir to my work when I left, so it just sits, waiting for someone to love it...and to interpret my awful organometallic lab notebook (which is another regret...)</description>
		<content:encoded><![CDATA[<p>Excimer- I am also a huge fan of Ni(dppe)Cl2. It is cheap, and it is falling-off-a-log easy to make. </p>
<p>I had the luxury in graduate school to work in two groups, one organic materials and one organometallic. Since my advisor was untenured at the time, I had to have a tenured co-advisor. I think in most cases at my alma mater, this is purely a formality, but my projects had enough overlap that I got to do some real organometallic work. </p>
<p>The pentacene stuff killed off some really neat projects and brought my organometallic work to an abrupt halt. I made some really nifty 1,2 disubstituted ferrocenes, really cool compounds by 2 different and interesting routes, that never made it into print, which is one of my only regrets from grad school. There was not an obvious heir to my work when I left, so it just sits, waiting for someone to love it&#8230;and to interpret my awful organometallic lab notebook (which is another regret&#8230;)</p>
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		<title>By: GMC2007</title>
		<link>http://www.coronene.com/blog/?p=186&#038;cpage=1#comment-1721</link>
		<dc:creator>GMC2007</dc:creator>
		<pubDate>Thu, 11 Oct 2007 19:28:00 +0000</pubDate>
		<guid isPermaLink="false">http://www.coronene.com/blog/?p=186#comment-1721</guid>
		<description>An off-topic comment.  Thought you might like to know that I linked CBC in the latest Crapshoot (the first in a 3-part look at rotatable bonds).  Also congratulations on your paper and CBC&#039;s first birthday.</description>
		<content:encoded><![CDATA[<p>An off-topic comment.  Thought you might like to know that I linked CBC in the latest Crapshoot (the first in a 3-part look at rotatable bonds).  Also congratulations on your paper and CBC&#8217;s first birthday.</p>
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		<title>By: Excimer</title>
		<link>http://www.coronene.com/blog/?p=186&#038;cpage=1#comment-1718</link>
		<dc:creator>Excimer</dc:creator>
		<pubDate>Thu, 11 Oct 2007 13:17:00 +0000</pubDate>
		<guid isPermaLink="false">http://www.coronene.com/blog/?p=186#comment-1718</guid>
		<description>David, I like nickel catalysts.  Ni(dppe)Cl2 is a very pretty red and like less than half the price of most Pd catalysts. I enjoy using them.</description>
		<content:encoded><![CDATA[<p>David, I like nickel catalysts.  Ni(dppe)Cl2 is a very pretty red and like less than half the price of most Pd catalysts. I enjoy using them.</p>
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