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Rational design and synthesize steri...

Rutgers The State University of New Jersey - New Brunswick.

Rational design and synthesize sterically less hindered pincer-iridium catalysts for alkane dehydrogenation.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	Rational design and synthesize sterically less hindered pincer-iridium catalysts for alkane dehydrogenation.
作者:	Zheng, Yang.
面頁冊數:	59 p.
附註:	Source: Masters Abstracts International, Volume: 55-02.
附註:	Adviser: Alan S. Goldman.
Contained By:	Masters Abstracts International55-02(E).
標題:	Inorganic chemistry.
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=1603624
ISBN:	9781339230023

Rational design and synthesize sterically less hindered pincer-iridium catalysts for alkane dehydrogenation.
Zheng, Yang.

Rational design and synthesize sterically less hindered pincer-iridium catalysts for alkane dehydrogenation. - 59 p.

Source: Masters Abstracts International, Volume: 55-02.

Thesis (M.S.)--Rutgers The State University of New Jersey - New Brunswick, 2015.

Dehydrogenation of alkane, which can convert alkane to alkene effectively and atom economically, is one of the most important and challenge goal in modern catalysis since the dehydrogenation product, alkenes, are ubiquitous as reagents and intermediates for a variety of useful transformation. Our group focused on the development of PCP Iridium catalysts for alkane dehydrogenation in the last decades and made lots of significant breakthroughs. One of them was that we found the steric hindrance of the PCP ligand backbone can affect the activity of the catalysts for dehydrogenation of alkane observably. The work presented in this thesis studied one new sterically less hindered pincer-ligated Iridium complex, (tBu2PCPMe2)IrH4, as the perfection of the study of the steric effect of PCP Iridium complexes for alkane dehydrogenation.

ISBN: 9781339230023Subjects--Topical Terms:

708705
Inorganic chemistry.

Rational design and synthesize sterically less hindered pincer-iridium catalysts for alkane dehydrogenation.
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245 1 0 $a Rational design and synthesize sterically less hindered pincer-iridium catalysts for alkane dehydrogenation.
300 $a 59 p.
500 $a Source: Masters Abstracts International, Volume: 55-02.
500 $a Adviser: Alan S. Goldman.
502 $a Thesis (M.S.)--Rutgers The State University of New Jersey - New Brunswick, 2015.
520 $a Dehydrogenation of alkane, which can convert alkane to alkene effectively and atom economically, is one of the most important and challenge goal in modern catalysis since the dehydrogenation product, alkenes, are ubiquitous as reagents and intermediates for a variety of useful transformation. Our group focused on the development of PCP Iridium catalysts for alkane dehydrogenation in the last decades and made lots of significant breakthroughs. One of them was that we found the steric hindrance of the PCP ligand backbone can affect the activity of the catalysts for dehydrogenation of alkane observably. The work presented in this thesis studied one new sterically less hindered pincer-ligated Iridium complex, (tBu2PCPMe2)IrH4, as the perfection of the study of the steric effect of PCP Iridium complexes for alkane dehydrogenation.
520 $a (tBu2PCPMe2)IrH4 is the least steric PCP Iridium complex we have every made. It was expected to have all the advantage as another small steric complex (tBu2Me2PCP)IrH4, which had shown very high reactivity for alkane dehydrogenation but was hard to synthesis. (tBu2PCPMe2)IrH4 has the comparable satiric and electronic effects as (tBu2Me2PCP)IrH4 and is relatively easier to synthesis compared with the latter. What's more, without the â-H in Me2- side, the stability of complex may be improved due to the less chance undergoing Cyclometalation. As such, ( tBu2PCPMe2)IrH4 is a good complex to study the steric effect of PCP Iridium complexes for alkane dehydrogenation.
520 $a tBu2PCPMe2-H ligand was successfully synthesized by a revised procedure. The corresponding Iridium complexes (tBu2PCP Me2)IrH4 and (tBu2PCPMe2)Ir(C 2H4) were made as well. Addition of small molecules, H 2, N2, CO, to (tBu2PCPMe2)IrH 4 and (tBu2PCPMe2)Ir(C2H 4) was then studied to investigate the properties of such complexes. The alkane transfer dehydrogenation of cyclooctane by (tBu2PCP Me2)IrH4 and (tBu2PCPMe2)Ir(C 2H4) was studied to compare the activity of this new complex with our previous PCP Iridium catalysts. Finally, the effect of different acceptor and the effect of acceptor's concentration were also studied.
590 $a School code: 0190.
650 4 $a Inorganic chemistry. $3 708705
650 4 $a Organic chemistry. $3 708640
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690 $a 0490
710 2 $a Rutgers The State University of New Jersey - New Brunswick. $3 212684
773 0 $t Masters Abstracts International $g 55-02(E).
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791 $a M.S.
792 $a 2015
793 $a English
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