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±¾Ìû²úÉú 1 ¸ö ·­ÒëEPI £¬µã»÷ÕâÀï½øÐв鿴

donglijie

Òø³æ (³õÈëÎÄ̳)

[ÇóÖú] Conventional and Unconventional MetalOrganic Frameworks Based

The class of materials known as metalorganic frameworks,
or MOFs, is the subject of an enormous amount of current
research. The other reviews in this issue serve as testament to this
fact. The defining character of these compounds is their porosity,
which can be tuned by changing the geometry and size of the
carboxylic acid ligands. In the early years of this research,
carboxylate-based MOFs were designed to have ever-greater
surface areas, resulting in the astonishing increase from 600
to >5000 m2/g.16 In addition, interest was keyed toward very
large uptake of certain gases such as hydrogen, methane, and
carbon dioxide and the possibility of a range of potential gas
separations. The number of reported MOFs has skyrocketed as
researchers have explored the vast number of possible combinations
of ligand design, transition metals, coligands, and structuredirecting
agents. Many investigators were fascinated by the idea
that one could use a set of principles to define structures that
would be porous. However, although many papers claim to have
created porous products, the structural data is insufficient. One
must have a sorption isotherm to prove the extent of porosity.
Carboxylate-based MOFs have been shown to have remarkably
high surface area and uniform pore size distribution, but
their lack of stability in air and water poses a significant problem if
they are to be used in industrial or commercial applications.
Divalent metal carboxylates are subject to hydrolysis and usuallyquite soluble in acid solution. It should be pointed out that other
types of MOFs, such as those based on pyrazolate ligands, can be
much more robust.7 Phosphonates form stronger bonds than
carboxylates do with metal atoms, so it is natural that investigators
should try to prepare phosphonate-based MOFs. From our
own experience, monovalent metal phosphonates are highly
soluble, even though they may crystallize as supramolecular
structures. As the valence of the metal increases, the solubility
decreases. Divalent metal phosphonates are soluble enough that
single crystals can be obtained by hydrothermal or solvothermal
techniques, whereas trivalent and tetravalent metal phosphonates
are rarely crystalline as they are highly insoluble and tend
to precipitate as poorly ordered layered materials. The tetravalent
metal phosphonates are insoluble even in strong acid solution.
Phosphonates have three oxygen atoms capable of bonding
to metals. They can also coordinate metals when they are in any
state of protonation. This results in many possible modes of cocoordination
and myriad different arrangements that the structures
can take, many of which are not porous and therefore not MOFs.
The majority of metal phosphonate compounds are not MOFs,
and although there are a number of instances where phosphonate-
based MOFs have been prepared, they were generally not
by design. The interested reader is directed to a recently released
book for more information.

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hookhans

Ìú¸Ëľ³æ (ÖøÃûдÊÖ)

Farmer

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phu_grassman: ½ð±Ò+5, thanks 2013-03-11 16:23:05
donglijie: ½ð±Ò+100, ·­ÒëEPI+1, ¡ï¡ï¡ï¡ï¡ï×î¼Ñ´ð°¸ 2013-03-11 16:46:15
½ðÊôÓлú¹Ç¼Ü»¯ºÏÎ¼´MOFs£¬ÊÇĿǰͶÈë´óÁ¿Ñо¿µÄÒ»Àà²ÄÁÏ¡£ ÔÚÕâ·½ÃæµÄ£¨´óÁ¿)ÆäËü×ÛÊö¿ÉÒÔ×÷ΪÕâÒ»½áÂÛµÄ×ôÖ¤¡£ÕâЩ»¯ºÏÎïµÄÈ·¶¨ÌØÕ÷ÊÇËüÃǾßÓеĿ×ÐÔ£¬¿ÉÒÔͨ¹ý¸ÄôÈËá»ùÅäÌåµÄ¼¸ºÎ½á¹¹ºÍ³ß´çÀ´µ÷±ä¡£ÔÚÔçЩÄêµÄÑо¿ÖУ¬ôÈ»ùµÄMOFsÑо¿Ö÷Òª³¯ÏòÉè¼ÆÇ°ËùûÓеıíÃæ»ý£¬½á¹ûÆä±íÃæ»ýµÃµ½¾ªÈ˵ÄÌá¸ß£¬´Ó600 to >5000 m2/g. ´ËÍ⣬ Ñо¿ÐËȤ»¹¼¯ÖÐÔÚÆä´óÁ¿ÎüÊÕÒ»Ð©ÆøÌåÉÏ£¬±ÈÈ磬 ÇâÆø¡¢¼×Íé¡¢¶þÑõ»¯Ì¼£¬ÒÔ¼°ÆäÓÃÓÚÆøÌå·ÖÀëµÄDZÔÚ¿ÉÄÜÐÔ¡£ Ëæ×ÅÑо¿ÈËÔ±·¢¾ò³ö´óÁ¿ÅäÌåÉè¼Æ¡¢¹ý¶È½ðÊô¡¢¹²ÅäÌå¡¢½á¹¹µ¼Ïò¼ÁÖ®¼äµÄ¿ÉÐÐÐÔ×éºÏ·½·¨£¬ÓйØMFOsµÄ±¨µÀÊýÁ¿¼±¾çì­Éý¡£ºÜ¶àÑо¿ÕßÂú×ãÓÚÄܹ»ÓÃһϵÁеļȶ¨·½·¨À´È·¶¨½á¹¹µÄ¿×µÀÐÔ¡£ È»¶ø£¬¾¡¹ÜºÜ¶àÎÄÕÂÉùÃ÷ËûÃǹ¹½¨ÁË¿×ÐÔ²ÄÁÏ£¬µ«Êǽṹ·½ÃæµÄÊý¾Ý»¹ÊÇǷȱ¡£¿×ÐÔ±ØÐëÓÃÎü¸½ÇúÏßÀ´Ö¤Ã÷¡£ôÈËá»ùµÄMOFs ÒѾ­ÏÔʾÆä¾ßÓоªÈ˵ĸ߱íÃæ»ýºÍ¾ùÒ»µÄ¿×³ß´ç·Ö²¼£¬µ«ÊÇÓÉÓÚËüÃÇÔÚ¿ÕÆø»òË®ÖÐȱ·¦Îȶ¨ÐÔ£¬Òò´ËÔÚ¹¤Òµ»òÉÌÒµ»¯Ó¦ÓÃÖÐÓöµ½ºÜ´óµÄÎÊÌâ¡£¶þ¼Û½ðÊôµÄôÈËáͨ³£ÔÚËáÐÔÈÜÒºÖÐË®½â£¬²¢ÇÒºÜÎȶ¨¡£ Ó¦¸ÃÖ¸³öµÄÊÇ£¬ ÆäËüÀàÐ͵Ġ MOFs, ±ÈÈçÄÇЩ»ùÓÚßÁßòÌØ»ùÅäÌåµÄMOFs, ¿ÉÒÔ¸üÎȶ¨´æÔÚ¡£ÒòΪÁ×Ëá»ù±ÈôÈËá»ùÄÜÓë½ðÊô³É¸üÇ¿µÄ¼ü£¬Òò´ËÑо¿ÕßÃdz¢ÊÔÖÆ±¸Á×Ëá»ùµÄMOFsÊÇ×ÔÈ»¶øÈ»µÄÊÂÇé¡£ ´ÓÎÒÃǵÄʵÑéÀ´¿´£¬ µ¥¼ÛµÄ½ðÊôÁ×Ëá¾ßÓиßÈܽâÐÔ£¬¾¡¹ÜËüÃÇ»áÒÔ³¬·Ö×ӽṹµÄÐÎʽ½á¾§¡£Ëæ×ŽðÊô¼Û̬µÄÔö¼Ó£¬ÈܽâÐÔ½µµÍ¡£¶þ¼Û½ðÊôÁ×Ëá¾ßÓÐ×ã¹»µÄÈܽâÐÔ£¬Äܹ»Í¨¹ýË®ÈÈ»òÈܼÁÈȵļ¼ÊõµÃµ½µ¥¾§£»¶øÈý¼ÛºÍËļ۵ĽðÊôÁ×ËáºÜÉٽᾧ£¬ÒòΪËüÃÇÈܽâÐԺܲͨ³£Ç÷ÏòÓÚÐγÉÎÞÐòµÄ²ã×´½á¹¹²ÄÁÏ¡£Èý¼ÛºÍËļ۵ĽðÊôÁ×ËáÉõÖÁ²»ÈÜÓÚÇ¿Ëá¡£Á×Ëá¾ßÓÐÈý¸ö¿ÉÒԺͽðÊô³É¼üµÄÑõÔ­×Ó£¬ ËüÃÇÉõÖÁÔÚÈκÎÖÊ×Ó»¯×´Ì¬ÏÂÈÔÄܺͽðÊôÅäλ¡£Õâ¾Íµ¼Ö²ÄÁϽṹ¿ÉÒÔ²ÉÈ¡ºÜ¶àµÄ¿ÉÄÜÅäλģÐͺʹóÁ¿µÄ²»Í¬µÄ×éºÏ£¬¶øÆäÖеĺܶà½á¹¹²»ÊÇ¿×ÐԵģ¬Òò´Ë²»ÊÇMOFs¡£ ´ó¶àÊý½ðÊôÁ×ËữºÏÎï²»ÊÊMOFs£¬ ¾¡¹ÜÓÐһЩÀý×Ó±¨µÀËµÖÆ±¸ÁËÁ×Ëá»ùµÄMOFs£¬ µ«ÊÇËüÃǶ¼²»ÊÇͨ¹ýÉè¼Æ»ñµÃµÄ¡£ ¸ü¶àÐÅÏ¢£¬¸ÐÐËȤµÄ¶ÁÕß¿ÉÒԲο¼×î½ü·¢²¼µÄÒ»±¾Êé¡£
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