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  <titleInfo>
    <title>Intrinsically microporous polyimides derived from norbornane-2-spiro-?-cyclopentanone-??-spiro-2?-norbornane-5,5?,6,6?-tetracarboxylic dianhydride</title>
  </titleInfo>
  <name type="personal">
    <namePart>Lu Y.</namePart>
  </name>
  <name type="personal">
    <namePart>Hu X.</namePart>
  </name>
  <name type="personal">
    <namePart>Pang Y.</namePart>
  </name>
  <name type="personal">
    <namePart>Miao J.</namePart>
  </name>
  <name type="personal">
    <namePart>Zhao J.</namePart>
  </name>
  <name type="personal">
    <namePart>Nie W.</namePart>
  </name>
  <name type="personal">
    <namePart>Wang Z.</namePart>
  </name>
  <name type="personal">
    <namePart>Yan J.</namePart>
  </name>
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    <issuance>monographic</issuance>
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  <abstract>Here, a series of intrinsically microporous polyimides (PIM-PIs) were prepared from norbornane-2-spiro-?-cyclopentanone-??-spiro-2?-norbornane-5,5?,6,6?-tetracarboxylic dianhydride (CpODA) and archetypal contorted diamines, and their microstructures and gas transport properties were systematically investigated and compared with those of the counterparts derived from 4,4'-(hexafluoroisopropylidene)diphthalic anhydride (6FDA). For certain diamines, the surface areas, interchain distances, and fractional free volumes (FFV) of the CpODA-derived PIM-PIs were considerably greater than those of the 6FDA-derived ones, and were in the range of 92-567 m2 g?1, 0.575-0.607 nm, and 0.194-0.246, respectively. Consequently, the CpODA-derived PIM-PIs overall displayed higher gas permeabilities and better gas separation performances compared to the 6FDA-derived ones. In particular, CpODA-TBDA2 and CpODA-DAT showed high H2 permeabilities (&gt;600 Barrer) and moderate H2/N2 and H2/CH4 selectivities which approached or even surpassed the corresponding 2008 Robeson upper bounds. The excellent gas separation performance of these CpODA-derived PIM-PIs may be attributed to the contorted and bulky architecture of the CpODA residue, which led to reduced inter- and intra-molecular interactions and the formation of ultramicropores of &lt;0.7 nm. © 2021 Elsevier Ltd</abstract>
  <subject>
    <topic>ALICYCLIC DIANHYDRIDE</topic>
  </subject>
  <subject>
    <topic>GAS SEPARATION PERFORMANCE</topic>
  </subject>
  <subject>
    <topic>INTERCHAIN DISTANCE</topic>
  </subject>
  <subject>
    <topic>POLYIMIDES OF INTRINSIC MICROPORE</topic>
  </subject>
  <subject>
    <topic>STRUCTURE-PROPERTY RELATIONSHIP</topic>
  </subject>
  <relatedItem type="series">
    <titleInfo>
      <title>Polymer. 228, 123955, 2021, DOI: 10.1016/j.polymer.2021.123955</title>
    </titleInfo>
  </relatedItem>
  <identifier type="uri">https://drive.google.com/file/d/1ymuWioxyN0IVCTaH905zXc-R7z2cwb8h/view?usp=drive_link</identifier>
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