2004
DOI: 10.1016/j.polymer.2004.07.005
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Packing mode and conformational transition of alkyl side chains in N-alkylated poly(p-benzamide) comb-like polymer

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Cited by 84 publications
(87 citation statements)
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“…Note that the reported T m of PABA 17 (with a 97% degree of substituents), prepared by alkylation of poly(p-benzamide) with sodium hydride, was 3 1C, which was unexpectedly lower than that of n-hexadecane (T m ¼22 1C). 40 The authors attributed this reason to the difficult packing of PABA 17 because of the bulky phenylene groups. However, in our case, PABA 17 (with a 100% degree of substituents) melts at 31 1C, which indicates that only a 3% deficit in the introduction of alkyl side chains significantly decreases side-chain crystallinity for PABA 17 .…”
Section: Thermal Properties Of Pabasmentioning
confidence: 99%
See 1 more Smart Citation
“…Note that the reported T m of PABA 17 (with a 97% degree of substituents), prepared by alkylation of poly(p-benzamide) with sodium hydride, was 3 1C, which was unexpectedly lower than that of n-hexadecane (T m ¼22 1C). 40 The authors attributed this reason to the difficult packing of PABA 17 because of the bulky phenylene groups. However, in our case, PABA 17 (with a 100% degree of substituents) melts at 31 1C, which indicates that only a 3% deficit in the introduction of alkyl side chains significantly decreases side-chain crystallinity for PABA 17 .…”
Section: Thermal Properties Of Pabasmentioning
confidence: 99%
“…The heat of fusion per monomeric unit of PABA 17 determined by DSC was À36.8 J g À1 , which is comparable with the reported value of comb polyamides. 40,41 X-ray scattering study of PABAs The packing mode of PABA n was investigated using WAXD measurements. Figure 5 depicts the WAXD patterns and profiles with a reciprocal lattice of PABA n polymers.…”
Section: Thermal Properties Of Pabasmentioning
confidence: 99%
“…9). In an experimental study, it was shown that the closed packing was hindered by the presence of the bulky side-chains [36]. This result indirectly supports that the backbone becomes more dominant when the number of the repeating units of PPP and PPy increased.…”
Section: Resultsmentioning
confidence: 80%
“…Since the discovery that PP conducts electricity when doped with oxidizing or reducing agents [4], a great deal of research has gone into the study of this material and its derivatives [5][6][7]. The effect of side chain chemistry and side chain length on the planarity of PP backbones has been extensively investigated by various groups [8][9][10][11].…”
Section: Introductionmentioning
confidence: 99%
“…One of the most common methods for the synthesis of polyarylenes [14] is the cross-coupling of aryl halides and aryl boronic acids (Suzuki coupling) [11] that has several advantages, such as simplicity of the procedure and insensitivity of the reaction to moisture. Furthermore, this coupling reaction can be applied to monomers carrying functional groups [15].…”
Section: Introductionmentioning
confidence: 99%