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[M3(mu3-O)(O2CR)6] and Related Trigo...

Schoedel, Alexander.

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[M3(mu3-O)(O2CR)6] and Related Trigonal Prisms: Versatile Molecular Building Blocks for 2-Step Crystal Engineering of Functional Metal-Organic Materials.

紀錄類型:	書目-電子資源 : Monograph/item
正題名/作者:	[M3(mu3-O)(O2CR)6] and Related Trigonal Prisms: Versatile Molecular Building Blocks for 2-Step Crystal Engineering of Functional Metal-Organic Materials./
作者:	Schoedel, Alexander.
面頁冊數:	273 p.
附註:	Source: Dissertation Abstracts International, Volume: 75-07(E), Section: B.
Contained By:	Dissertation Abstracts International75-07B(E).
標題:	Inorganic chemistry. -
電子資源:	http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3615951
ISBN:	9781303825156

[M3(mu3-O)(O2CR)6] and Related Trigonal Prisms: Versatile Molecular Building Blocks for 2-Step Crystal Engineering of Functional Metal-Organic Materials.
Schoedel, Alexander.

[M3(mu3-O)(O2CR)6] and Related Trigonal Prisms: Versatile Molecular Building Blocks for 2-Step Crystal Engineering of Functional Metal-Organic Materials. - 273 p.

Source: Dissertation Abstracts International, Volume: 75-07(E), Section: B.

Thesis (Ph.D.)--University of South Florida, 2014.

This item is not available from ProQuest Dissertations & Theses.

Metal-organic materials (MOMs) assembled from metal-based building blocks and organic linkers have attracted much interest due to their large pore dimensions and their enormous structural diversity. In comparison to their inorganic counterparts (zeolites), these crystalline materials can be easily modified to tailor pore dimensions and functionality for specifically targeted properties.

ISBN: 9781303825156Subjects--Topical Terms:

3173556
Inorganic chemistry.

[M3(mu3-O)(O2CR)6] and Related Trigonal Prisms: Versatile Molecular Building Blocks for 2-Step Crystal Engineering of Functional Metal-Organic Materials.
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245 1 0 $a [M3(mu3-O)(O2CR)6] and Related Trigonal Prisms: Versatile Molecular Building Blocks for 2-Step Crystal Engineering of Functional Metal-Organic Materials.
300 $a 273 p.
500 $a Source: Dissertation Abstracts International, Volume: 75-07(E), Section: B.
500 $a Adviser: Michael J. Zaworotko.
502 $a Thesis (Ph.D.)--University of South Florida, 2014.
506 $a This item is not available from ProQuest Dissertations & Theses.
520 $a Metal-organic materials (MOMs) assembled from metal-based building blocks and organic linkers have attracted much interest due to their large pore dimensions and their enormous structural diversity. In comparison to their inorganic counterparts (zeolites), these crystalline materials can be easily modified to tailor pore dimensions and functionality for specifically targeted properties.
520 $a The work presented herein encompasses the development of a synthetic 2-step process for the construction of novel families of MOMs or 'platforms' and allow us exquisite design and control over the resulting network topologies. Examples of cationic mesoporous structures were initially exploited, containing carboxylate based centers connected by metal-pyridine bonds. The inherently cationic nets allowed for subsequent anion exchange which can be regarded as an elegant and easy postsynthetic modification strategy. The incorporation of different functionalities inside the channels of the networks was then demonstrated as useful in terms of carbon dioxide capture.
520 $a The scope of the 2-step process was then expanded to construction of the first trinodal MOM platform involving triangular, tetrahedral and trigonal prismatic building units: tp-PMBB-1-asc. Examples of reticular chemistry are shown which enable the formation of large and functionalized nanocages with retention of the underlying network topology. Gas adsorption studies indicate relatively high uptakes of carbon dioxide and hydrogen which, together with the use of inexpensive ligands, provide an excellent cost/performance ratio of these materials. Moreover, very high stability in organic solvents and especially in water are addressed which is a particularly challenging, but industrially relevant target in the field of Metal-Organic Materials.
520 $a The 2-step approach was also used to synthesize a new and versatile class of metal-organic materials with augmented lonsdaleite-e (lon-e-a) topology. This family of lon-e nets is built by pillaring of hexagonal 2-dimensional kagome (kag) lattices that are in turn pillared by a trigonal prismatic Primary Molecular Building Block (tp-PMBB-1). These MOMs represent the first examples of axial-to-axial-pillared undulating kag layers and they are readily fine-tuned because the bdc2- moieties can be varied at their 5-position without changing the overall structure. This lon-e platform possesses functionalized hexagonal channels since the kag lattices are necessarily eclipsed. The effect of the substituent at the 5-positions of the bdc2- linkers upon gas adsorption, particularly the heats of adsorption of carbon dioxide and methane, were studied.
520 $a If linear dicarboxylates were instead utilized, we were able to synthesize a new and versatile class of metal-organic materials that exhibits 4,6-connected fsb topology. These networks are constructed from simple and inexpensive building units and since interpenetration is precluded, afford very high void volumes. They therefore represent ideal targets to generate a novel family of frameworks, because of the ready availability functionalized and expanded ligand derivatives. They also allow for systematic fine tuning and could ultimately provide a roadmap to ultra-high surface areas from simple building blocks.
590 $a School code: 0206.
650 4 $a Inorganic chemistry. $3 3173556
650 4 $a Materials science. $3 543314
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710 2 $a University of South Florida. $b Chemistry. $3 2093640
773 0 $t Dissertation Abstracts International $g 75-07B(E).
790 $a 0206
791 $a Ph.D.
792 $a 2014
793 $a English
856 4 0 $u http://pqdd.sinica.edu.tw/twdaoapp/servlet/advanced?query=3615951