High Glass Transition and Optical Transparency of Novel Organosoluble Polyamides Containing 4-tert-Butyltoluene Moiety
A series of novel polyamides 3a-3d containing 4-tert-butyltoluene moiety, were prepared using the phosphorylation polycondensation technique. FT-IR and 1↑H NMR techniques were used to investigate the chemical structures of 3a-3d. The results confirmed that they agreed with the proposed structures fo...
Saved in:
Published in | Chinese journal of chemistry Vol. 29; no. 10; pp. 2197 - 2201 |
---|---|
Main Author | |
Format | Journal Article |
Language | English |
Published |
Weinheim
WILEY-VCH Verlag
01.10.2011
WILEY‐VCH Verlag Wiley Subscription Services, Inc |
Subjects | |
Online Access | Get full text |
ISSN | 1001-604X 1614-7065 |
DOI | 10.1002/cjoc.201180380 |
Cover
Abstract | A series of novel polyamides 3a-3d containing 4-tert-butyltoluene moiety, were prepared using the phosphorylation polycondensation technique. FT-IR and 1↑H NMR techniques were used to investigate the chemical structures of 3a-3d. The results confirmed that they agreed with the proposed structures for 3a-3d completely. The 3a-3d had inherent viscosities ranging from 0.71 to 1.67 dL·g^-1. All the polyamides showed excellent solubility, with the dissolvability at a concentration of 10 wt% in most amide polar solvents. Flexible and tough polyamide films could be prepared by casting from DMAc (N,N-dimethylacetamide) solvent. Their films were nearly colorless and exhibited high optical transparency, with the UV cutoff wavelength in the range of 346-363 nm and transmittance higher than 80% at 450 nm. They also exhibited high glass transition temperatures in the range of 310---343℃ and the onset decomposition temperatures in the range of 435-462 ℃ in nitrogen atmosphere. Meanwhile, these polyamide films possess good mechanical properties with tensile strengths of 76.4-86.1 MPa and elongations at break of 11.2%-27.3%. Due to those properties, these polyamides could be considered as photoelectric and microelectronic materials. |
---|---|
AbstractList | A series of novel polyamides 3a–3d containing 4‐tert‐butyltoluene moiety, were prepared using the phosphorylation polycondensation technique. FT‐IR and 1H NMR techniques were used to investigate the chemical structures of 3a–3d. The results confirmed that they agreed with the proposed structures for 3a–3d completely. The 3a–3d had inherent viscosities ranging from 0.71 to 1.67 dL·g−1. All the polyamides showed excellent solubility, with the dissolvability at a concentration of 10 wt% in most amide polar solvents. Flexible and tough polyamide films could be prepared by casting from DMAc (N,N‐dimethylacetamide) solvent. Their films were nearly colorless and exhibited high optical transparency, with the UV cutoff wavelength in the range of 346–363 nm and transmittance higher than 80% at 450 nm. They also exhibited high glass transition temperatures in the range of 310–343°C and the onset decomposition temperatures in the range of 435–462°C in nitrogen atmosphere. Meanwhile, these polyamide films possess good mechanical properties with tensile strengths of 76.4–86.1 MPa and elongations at break of 11.2%–27.3%. Due to those properties, these polyamides could be considered as photoelectric and microelectronic materials.
Based on a rigid aromatic diamine, α,α‐bis(4‐aminophenyl)‐4‐(t‐butyl)toluene (1), a series of novel polyamides 3a–3d containing 4‐tert‐butyltoluene moiety, were prepared successfully by a one‐step phosphorylation polycondensation technique. The obtained polyamides could be soluble in some solvents with the dissolvability at a concentration of 10 wt% at room temperature. Meanwhile, it showed high optical transparency with lcutoff in the range of 346–363 nm and T450 more than 80%. Moreover, the polyamides displayed sufficiently high Tg value beyond 310°C, and good mechanical properties. A series of novel polyamides 3a-3d containing 4-tert-butyltoluene moiety, were prepared using the phosphorylation polycondensation technique. FT-IR and 1H NMR techniques were used to investigate the chemical structures of3a-3d. The results confirmed that they agreed with the proposed structures for 3a-3dcompletely. The 3a-3d had inherent viscosities ranging from 0.71 to 1.67 dL·g-1. All the polyamides showed excellent solubility, with the dissolvability at a concentration of 10 wt% in most amide polar solvents. Flexible and tough polyamide films could be prepared by casting from DMAc (N,N-dimethylacetamide) solvent. Their films were nearly colorless and exhibited high optical transparency, with the UV cutoff wavelength in the range of 346-363 nm and transmittance higher than 80% at 450 nm. They also exhibited high glass transition temperatures in the range of 310-343°C and the onset decomposition temperatures in the range of 435-462°C in nitrogen atmosphere. Meanwhile, these polyamide films possess good mechanical properties with tensile strengths of 76.4-86.1 MPa and elongations at break of 11.2%-27.3%. Due to those properties, these polyamides could be considered as photoelectric and microelectronic materials. A series of novel polyamides 3a-3d containing 4-tert-butyltoluene moiety, were prepared using the phosphorylation polycondensation technique. FT-IR and 1↑H NMR techniques were used to investigate the chemical structures of 3a-3d. The results confirmed that they agreed with the proposed structures for 3a-3d completely. The 3a-3d had inherent viscosities ranging from 0.71 to 1.67 dL·g^-1. All the polyamides showed excellent solubility, with the dissolvability at a concentration of 10 wt% in most amide polar solvents. Flexible and tough polyamide films could be prepared by casting from DMAc (N,N-dimethylacetamide) solvent. Their films were nearly colorless and exhibited high optical transparency, with the UV cutoff wavelength in the range of 346-363 nm and transmittance higher than 80% at 450 nm. They also exhibited high glass transition temperatures in the range of 310---343℃ and the onset decomposition temperatures in the range of 435-462 ℃ in nitrogen atmosphere. Meanwhile, these polyamide films possess good mechanical properties with tensile strengths of 76.4-86.1 MPa and elongations at break of 11.2%-27.3%. Due to those properties, these polyamides could be considered as photoelectric and microelectronic materials. A series of novel polyamides 3a – 3d containing 4‐ tert‐ butyltoluene moiety, were prepared using the phosphorylation polycondensation technique. FT‐IR and 1 H NMR techniques were used to investigate the chemical structures of 3a–3d . The results confirmed that they agreed with the proposed structures for 3a – 3d completely. The 3a – 3d had inherent viscosities ranging from 0.71 to 1.67 dL·g −1 . All the polyamides showed excellent solubility, with the dissolvability at a concentration of 10 wt% in most amide polar solvents. Flexible and tough polyamide films could be prepared by casting from DMAc ( N , N ‐dimethylacetamide) solvent. Their films were nearly colorless and exhibited high optical transparency, with the UV cutoff wavelength in the range of 346–363 nm and transmittance higher than 80% at 450 nm. They also exhibited high glass transition temperatures in the range of 310–343°C and the onset decomposition temperatures in the range of 435–462°C in nitrogen atmosphere. Meanwhile, these polyamide films possess good mechanical properties with tensile strengths of 76.4–86.1 MPa and elongations at break of 11.2%–27.3%. Due to those properties, these polyamides could be considered as photoelectric and microelectronic materials. |
Author | Wang, Chenyi Li, Guang Jiang, Jianming Zhao, Xiaoyan |
AuthorAffiliation | Changzhou Key Laboratory for Polymer Materials, School of Material Science and Engineering, Changzhou University, Changzhou, Guangdong 213164, China School of Petrochemical Engineering, Changzhou University, Changzhou, Guangdong 213164, China State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Material Science and Engineering, Donghua University, Shanghai 201620, China |
Author_xml | – sequence: 1 fullname: 汪称意 赵晓燕 李光 江建明 |
BookMark | eNqFkE1v1DAQhi3USvSDK2cjzln8ETvJESK6C2p3QWpVxMVyvJOtl9Te2t6W_Pu6SrXixmlGo-eZGb2n6Mh5Bwi9p2RGCWGfzNabGSOU1oTX5A06oZKWRUWkOMo9IbSQpPz1Fp3GuM18VTF5gh4XdnOH54OOEV8H7aJN1jus3RqvdskaPUzjnQ7gzIh9j5f-EQa8ChvtfPTDvhsA__DDqO_tGiJuvUvaOus2uCwShFR82adxSJkEB_jKW0jjOTru9RDh3Ws9QzcXX6_bRXG5mn9rP18WhlecFNBoRk0tRU9kJYWBkq45Y9BwqVnTCVn2hnWyXJeElHVGoe9MIxshek7qDvgZ-jjt3QX_sIeY1Nbvg8snFa2krInkQmZqNlEm-BgD9GoX7L0Oo6JEvWSrXrJVh2yz0EzCkx1g_A-t2u-r9l-3mFwbE_w9uDr8UbLilVC3y7maC0EvFsvf6mfmP7w-d-fd5iHnenB4UzPJpeDPU4ua7A |
Cites_doi | 10.1016/j.progpolymsci.2009.09.002 10.1007/s00396-009-2007-2 10.1007/s00289-009-0136-x 10.1002/cjoc.201090022 10.1002/pola.1990.080280604 10.1016/j.polymer.2007.08.041 10.1002/pola.20073 10.1016/j.polymdegradstab.2009.04.032 10.1002/pola.10426 10.1002/(SICI)1099-0518(20000501)38:9<1551::AID-POLA19>3.0.CO;2-O 10.1016/j.polymer.2004.09.030 10.1016/j.polymer.2004.03.037 10.1007/s00289-008-0013-z 10.1002/pol.1974.170120935 10.1002/(SICI)1097-4628(19990124)71:4<565::AID-APP7>3.0.CO;2-P 10.1016/j.polymer.2005.11.064 10.1002/(SICI)1099-0518(19960715)34:9<1663::AID-POLA3>3.0.CO;2-T 10.1002/cjoc.200990378 |
ContentType | Journal Article |
Copyright | Copyright © 2011 SIOC, CAS, Shanghai & WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim Copyright © 2011 SIOC, CAS, Shanghai & WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim |
Copyright_xml | – notice: Copyright © 2011 SIOC, CAS, Shanghai & WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim – notice: Copyright © 2011 SIOC, CAS, Shanghai & WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim |
DBID | 2RA 92L CQIGP ~WA BSCLL AAYXX CITATION |
DOI | 10.1002/cjoc.201180380 |
DatabaseName | 维普期刊资源整合服务平台 中文科技期刊数据库-CALIS站点 维普中文期刊数据库 中文科技期刊数据库- 镜像站点 Istex CrossRef |
DatabaseTitle | CrossRef |
DatabaseTitleList | CrossRef |
DeliveryMethod | fulltext_linktorsrc |
Discipline | Chemistry |
DocumentTitleAlternate | High Glass Transition and Optical Transparency of Novel Organosoluble Polyamides Containing 4-tert-Butyltoluene Moiety |
EISSN | 1614-7065 |
EndPage | 2201 |
ExternalDocumentID | 3957965841 10_1002_cjoc_201180380 CJOC201180380 ark_67375_WNG_G551FHNZ_Q 39826365 |
Genre | shortCommunication |
GrantInformation_xml | – fundername: the Opening Project of State Key Laboratory for Modification of Chemical Fibers and Polymer Materials funderid: LK1001 – fundername: the National Natural Science Foundation of China funderid: 51103016 – fundername: the Grant‐in‐aid for Youth Innovation Fund from Changzhou University funderid: ZMF11020017 and ZMF1002106 |
GroupedDBID | .3N .GA .Y3 05W 0R~ 10A 1L6 1OB 1OC 29B 2RA 31~ 33P 3SF 3WU 4.4 50Y 50Z 51W 51X 52M 52N 52O 52P 52S 52T 52U 52W 52X 53G 5GY 5VR 5VS 66C 702 7PT 8-0 8-1 8-3 8-4 8-5 8UM 92L AAESR AAEVG AAHHS AANLZ AAONW AASGY AAXRX AAZKR ABCQN ABCUV ABDBF ABEML ABHUG ABIJN ABJNI ABPVW ACAHQ ACBWZ ACCFJ ACCZN ACGFS ACIWK ACPOU ACSCC ACXBN ACXME ACXQS ADAWD ADBBV ADDAD ADEOM ADIZJ ADKYN ADMGS ADOZA ADXAS ADZMN ADZOD AEEZP AEIGN AEIMD AENEX AEQDE AEUQT AEUYR AFBPY AFFPM AFGKR AFPWT AFRAH AFUIB AFVGU AGJLS AHBTC AIURR AIWBW AJBDE AJXKR ALAGY ALMA_UNASSIGNED_HOLDINGS ALUQN AMBMR AMYDB ATUGU AUFTA AZBYB AZFZN AZVAB BAFTC BDRZF BFHJK BHBCM BMNLL BMXJE BNHUX BROTX BRXPI BY8 BZXJU CCEZO CDRFL CHBEP CQIGP CS3 CW9 D-E D-F DCZOG DPXWK DR2 DRFUL DRSTM EBS EJD F00 F01 F04 FA0 FEDTE G-S G.N GODZA H.T H.X HF~ HVGLF HZ~ IX1 J0M JPC LATKE LAW LC2 LC3 LEEKS LH4 LITHE LOXES LP6 LP7 LUTES LYRES MEWTI MK4 MRFUL MRSTM MSFUL MSSTM MXFUL MXSTM N04 N05 N9A NF~ O66 O9- P2W P4D PALCI Q.N Q11 QB0 QRW R.K RIWAO RJQFR RK2 RNS ROL RWI RX1 RYL SAMSI SUPJJ W8V W99 WBFHL WBKPD WIH WIK WOHZO WQJ WRC WXSBR WYISQ XG1 XV2 ZZTAW ~IA ~WA ~WT -SB -S~ 5XA 5XC AAXDM AITYG BSCLL CAJEB HGLYW OIG Q-- U1G U5L AAHQN AAMNL AANHP AAYCA ACRPL ACUHS ACYXJ ADNMO AFWVQ ALVPJ AAYXX AEYWJ AGHNM AGQPQ AGYGG CITATION TGP AAMMB AEFGJ AGXDD AIDQK AIDYY |
ID | FETCH-LOGICAL-c3730-e9a21c865f06765ce41d322e936a29b564fc2b64d4004821cefbc96955f308be3 |
IEDL.DBID | DR2 |
ISSN | 1001-604X |
IngestDate | Fri Jul 25 11:09:06 EDT 2025 Tue Jul 01 03:35:09 EDT 2025 Wed Jan 22 17:10:40 EST 2025 Wed Oct 30 09:59:52 EDT 2024 Wed Feb 14 10:47:52 EST 2024 |
IsPeerReviewed | true |
IsScholarly | true |
Issue | 10 |
Language | English |
License | http://onlinelibrary.wiley.com/termsAndConditions#vor |
LinkModel | DirectLink |
MergedId | FETCHMERGED-LOGICAL-c3730-e9a21c865f06765ce41d322e936a29b564fc2b64d4004821cefbc96955f308be3 |
Notes | A series of novel polyamides 3a-3d containing 4-tert-butyltoluene moiety, were prepared using the phosphorylation polycondensation technique. FT-IR and 1↑H NMR techniques were used to investigate the chemical structures of 3a-3d. The results confirmed that they agreed with the proposed structures for 3a-3d completely. The 3a-3d had inherent viscosities ranging from 0.71 to 1.67 dL·g^-1. All the polyamides showed excellent solubility, with the dissolvability at a concentration of 10 wt% in most amide polar solvents. Flexible and tough polyamide films could be prepared by casting from DMAc (N,N-dimethylacetamide) solvent. Their films were nearly colorless and exhibited high optical transparency, with the UV cutoff wavelength in the range of 346-363 nm and transmittance higher than 80% at 450 nm. They also exhibited high glass transition temperatures in the range of 310---343℃ and the onset decomposition temperatures in the range of 435-462 ℃ in nitrogen atmosphere. Meanwhile, these polyamide films possess good mechanical properties with tensile strengths of 76.4-86.1 MPa and elongations at break of 11.2%-27.3%. Due to those properties, these polyamides could be considered as photoelectric and microelectronic materials. 31-1547/O6 Wang, Cheny Zhao, Xiaoyan Li, Guang Jiang, Jianrning (1. Changzhou Key Laboratory for Polymer Materials, School of Material Science and Engineering, Changzhou University, Changzhou, Guangdong 213164, China ;2. School of Petrochemical Engineering, Changzhou University, Changzhou, Guangdong 213164, China;3. State Key Laboratory for Modification of Chemical Fibers and Polymer Materials, College of Material Science and Engineering, Donghua University, Shanghai 201620, China) polyamides, solubility, optical transparency the Opening Project of State Key Laboratory for Modification of Chemical Fibers and Polymer Materials - No. LK1001 ark:/67375/WNG-G551FHNZ-Q the National Natural Science Foundation of China - No. 51103016 the Grant-in-aid for Youth Innovation Fund from Changzhou University - No. ZMF11020017 and ZMF1002106 ArticleID:CJOC201180380 istex:8FD8AF9AA0683FA50CCB0DD41F22AAB4A5D1A2B1 ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 |
PQID | 1766806356 |
PQPubID | 986331 |
PageCount | 5 |
ParticipantIDs | proquest_journals_1766806356 crossref_primary_10_1002_cjoc_201180380 wiley_primary_10_1002_cjoc_201180380_CJOC201180380 istex_primary_ark_67375_WNG_G551FHNZ_Q chongqing_primary_39826365 |
ProviderPackageCode | CITATION AAYXX |
PublicationCentury | 2000 |
PublicationDate | October, 2011 |
PublicationDateYYYYMMDD | 2011-10-01 |
PublicationDate_xml | – month: 10 year: 2011 text: October, 2011 |
PublicationDecade | 2010 |
PublicationPlace | Weinheim |
PublicationPlace_xml | – name: Weinheim – name: Shanghai |
PublicationTitle | Chinese journal of chemistry |
PublicationTitleAlternate | Chinese Journal of Chemistry |
PublicationYear | 2011 |
Publisher | WILEY-VCH Verlag WILEY‐VCH Verlag Wiley Subscription Services, Inc |
Publisher_xml | – name: WILEY-VCH Verlag – name: WILEY‐VCH Verlag – name: Wiley Subscription Services, Inc |
References | Liaw, D. J.; Chen, W. H.; Hu, C. K.; Lee, K. R.; Lai, J. Y.. Polymer, 2007, 48, 6571. Hsiao, S. H.; Yang, C. P.; Chen, S. H.. J. Polym. Sci., Part A: Polym. Chem., 2000, 38, 1551. Tan, J. H.; Wang, C. Y.; Peng, W. Y.; Li, G.; Jiang, J. M.. Polym. Bull., 2009, 62, 195. Wang, C. Y.; Zhao, X. Y.; Li, G.; Jiang, J. M.. Polym. Degrad. Stab., 2009, 94, 1526. Ge, Z. Y.; Yang, S. Y.; Tao, Z. Q.; Liu, J. G.; Fan, L.. Polymer, 2004, 45, 3627. In, I.; Kim, S. Y.. Polymer, 2006, 47, 547. Yamazaki, N.; Higashi, F.; Kawabata, J.. J. Polym. Sci., Part A: Polym. Chem. Ed., 1974, 12, 2149. Yang, C. P.; Hsiao, F. Z.. J. Polym. Sci., Part A: Polym. Chem., 2004, 42, 2272. Li, X. G.; Huang, M. R.. J. Appl. Polym. Sci., 1999, 71, 565. Li, X. G.; Huang, M. R., Advanced Materials Engineering of Liquid Crystalline Polymers, East China Normal University Press, Shanghai, China, 2000 (in Chinese). Yang, C. P.; Oishi, Y.; Kakimoto, M.; Imai, Y.. J. Polym. Sci., Part A: Polym. Chem., 1990, 28, 1353. Yamazaki, N.; Matsumoto, M.; Higashi, F.. J. Polym. Sci., Part A: Polym. Chem. Ed., 1975, 13, 1375. Cheng, L.; Jian, X. G.; Mao, S. Z.. J. Polym. Sci., Part A: Polym. Chem., 2002, 40, 3489. Hsiao, S. H.; Lin, K. H.. Polymer, 2004, 45, 7877. Wang, C. Y.; Li, G.; Jiang, J. M.. Chin. J. Chem., 2009, 27, 2255. Wang, C. Y.; Li, P. H.; Li, G.; Jiang, J. M.. Colloid Polym. Sci., 2009, 287, 495. Negi, Y. S.; Suzuki, Y. I.; Kawamura, I.; Kakimoto, M. A.; Imai, Y.. J. Polym. Sci., Part A: Polym. Chem., 1996, 34, 1663. Li, P. H.; Wang, C. Y.; Li, G.; Jiang, J. M.. Polym. Bull., 2010, 64, 127. Garcia, J. M.; Garcia, C. F.; Serna, F.; Pena, J. L. D.. Prog. Polym. Sci., 2010, 35, 623. Jiang, J. W.; Huang, S. P.; Liu, Y.; Sheng, S. R.; Huang, Z. Z.; Song, C. S.. Chin. J. Chem., 2010, 28, 102. 2010; 64 2004; 42 1974; 12 2009; 62 2000; 38 2010; 35 2000 1990; 28 2009; 94 2010; 28 2002; 40 2004; 45 2006; 47 1975; 13 2009; 287 1999; 71 2009; 27 1996; 34 2007; 48 Li X. G. (e_1_2_1_21_2) 2000 e_1_2_1_6_2 e_1_2_1_7_2 e_1_2_1_4_2 e_1_2_1_5_2 e_1_2_1_2_2 e_1_2_1_11_2 e_1_2_1_3_2 e_1_2_1_12_2 Yamazaki N. (e_1_2_1_19_2) 1975; 13 e_1_2_1_20_2 e_1_2_1_10_2 e_1_2_1_15_2 e_1_2_1_16_2 e_1_2_1_13_2 e_1_2_1_14_2 e_1_2_1_8_2 e_1_2_1_17_2 e_1_2_1_9_2 e_1_2_1_18_2 |
References_xml | – reference: Cheng, L.; Jian, X. G.; Mao, S. Z.. J. Polym. Sci., Part A: Polym. Chem., 2002, 40, 3489. – reference: Garcia, J. M.; Garcia, C. F.; Serna, F.; Pena, J. L. D.. Prog. Polym. Sci., 2010, 35, 623. – reference: Yamazaki, N.; Matsumoto, M.; Higashi, F.. J. Polym. Sci., Part A: Polym. Chem. Ed., 1975, 13, 1375. – reference: Li, P. H.; Wang, C. Y.; Li, G.; Jiang, J. M.. Polym. Bull., 2010, 64, 127. – reference: Hsiao, S. H.; Lin, K. H.. Polymer, 2004, 45, 7877. – reference: Wang, C. Y.; Li, P. H.; Li, G.; Jiang, J. M.. Colloid Polym. Sci., 2009, 287, 495. – reference: Jiang, J. W.; Huang, S. P.; Liu, Y.; Sheng, S. R.; Huang, Z. Z.; Song, C. S.. Chin. J. Chem., 2010, 28, 102. – reference: Yang, C. P.; Hsiao, F. Z.. J. Polym. Sci., Part A: Polym. Chem., 2004, 42, 2272. – reference: Li, X. G.; Huang, M. R.. J. Appl. Polym. Sci., 1999, 71, 565. – reference: Li, X. G.; Huang, M. R., Advanced Materials Engineering of Liquid Crystalline Polymers, East China Normal University Press, Shanghai, China, 2000 (in Chinese). – reference: Tan, J. H.; Wang, C. Y.; Peng, W. Y.; Li, G.; Jiang, J. M.. Polym. Bull., 2009, 62, 195. – reference: Wang, C. Y.; Li, G.; Jiang, J. M.. Chin. J. Chem., 2009, 27, 2255. – reference: Hsiao, S. H.; Yang, C. P.; Chen, S. H.. J. Polym. Sci., Part A: Polym. Chem., 2000, 38, 1551. – reference: Wang, C. Y.; Zhao, X. Y.; Li, G.; Jiang, J. M.. Polym. Degrad. Stab., 2009, 94, 1526. – reference: Yang, C. P.; Oishi, Y.; Kakimoto, M.; Imai, Y.. J. Polym. Sci., Part A: Polym. Chem., 1990, 28, 1353. – reference: Yamazaki, N.; Higashi, F.; Kawabata, J.. J. Polym. Sci., Part A: Polym. Chem. Ed., 1974, 12, 2149. – reference: Negi, Y. S.; Suzuki, Y. I.; Kawamura, I.; Kakimoto, M. A.; Imai, Y.. J. Polym. Sci., Part A: Polym. Chem., 1996, 34, 1663. – reference: In, I.; Kim, S. Y.. Polymer, 2006, 47, 547. – reference: Liaw, D. J.; Chen, W. H.; Hu, C. K.; Lee, K. R.; Lai, J. Y.. Polymer, 2007, 48, 6571. – reference: Ge, Z. Y.; Yang, S. Y.; Tao, Z. Q.; Liu, J. G.; Fan, L.. Polymer, 2004, 45, 3627. – volume: 40 start-page: 3489 year: 2002 publication-title: J. Polym. Sci., Part A: Polym. Chem. – volume: 48 start-page: 6571 year: 2007 publication-title: Polymer – volume: 287 start-page: 495 year: 2009 publication-title: Colloid Polym. Sci. – volume: 13 start-page: 1375 year: 1975 publication-title: J. Polym. Sci., Part A: Polym. Chem. Ed. – volume: 62 start-page: 195 year: 2009 publication-title: Polym. Bull. – volume: 94 start-page: 1526 year: 2009 publication-title: Polym. Degrad. Stab. – volume: 45 start-page: 3627 year: 2004 publication-title: Polymer – volume: 38 start-page: 1551 year: 2000 publication-title: J. Polym. Sci., Part A: Polym. Chem. – year: 2000 – volume: 45 start-page: 7877 year: 2004 publication-title: Polymer – volume: 34 start-page: 1663 year: 1996 publication-title: J. Polym. Sci., Part A: Polym. Chem. – volume: 27 start-page: 2255 year: 2009 publication-title: Chin. J. Chem. – volume: 64 start-page: 127 year: 2010 publication-title: Polym. Bull. – volume: 28 start-page: 1353 year: 1990 publication-title: J. Polym. Sci., Part A: Polym. Chem. – volume: 12 start-page: 2149 year: 1974 publication-title: J. Polym. Sci., Part A: Polym. Chem. Ed. – volume: 47 start-page: 547 year: 2006 publication-title: Polymer – volume: 71 start-page: 565 year: 1999 publication-title: J. Appl. Polym. Sci. – volume: 28 start-page: 102 year: 2010 publication-title: Chin. J. Chem. – volume: 42 start-page: 2272 year: 2004 publication-title: J. Polym. Sci., Part A: Polym. Chem. – volume: 35 start-page: 623 year: 2010 publication-title: Prog. Polym. Sci. – ident: e_1_2_1_3_2 doi: 10.1016/j.progpolymsci.2009.09.002 – ident: e_1_2_1_10_2 doi: 10.1007/s00396-009-2007-2 – ident: e_1_2_1_6_2 doi: 10.1007/s00289-009-0136-x – ident: e_1_2_1_5_2 doi: 10.1002/cjoc.201090022 – ident: e_1_2_1_12_2 doi: 10.1002/pola.1990.080280604 – ident: e_1_2_1_13_2 doi: 10.1016/j.polymer.2007.08.041 – ident: e_1_2_1_15_2 doi: 10.1002/pola.20073 – ident: e_1_2_1_17_2 doi: 10.1016/j.polymdegradstab.2009.04.032 – ident: e_1_2_1_8_2 doi: 10.1002/pola.10426 – ident: e_1_2_1_14_2 doi: 10.1002/(SICI)1099-0518(20000501)38:9<1551::AID-POLA19>3.0.CO;2-O – volume-title: Advanced Materials Engineering of Liquid Crystalline Polymers year: 2000 ident: e_1_2_1_21_2 – ident: e_1_2_1_7_2 doi: 10.1016/j.polymer.2004.09.030 – volume: 13 start-page: 1375 year: 1975 ident: e_1_2_1_19_2 publication-title: J. Polym. Sci., Part A: Polym. Chem. Ed. – ident: e_1_2_1_4_2 doi: 10.1016/j.polymer.2004.03.037 – ident: e_1_2_1_9_2 doi: 10.1007/s00289-008-0013-z – ident: e_1_2_1_18_2 doi: 10.1002/pol.1974.170120935 – ident: e_1_2_1_20_2 doi: 10.1002/(SICI)1097-4628(19990124)71:4<565::AID-APP7>3.0.CO;2-P – ident: e_1_2_1_11_2 doi: 10.1016/j.polymer.2005.11.064 – ident: e_1_2_1_2_2 doi: 10.1002/(SICI)1099-0518(19960715)34:9<1663::AID-POLA3>3.0.CO;2-T – ident: e_1_2_1_16_2 doi: 10.1002/cjoc.200990378 |
SSID | ssj0027726 |
Score | 1.8478848 |
Snippet | A series of novel polyamides 3a-3d containing 4-tert-butyltoluene moiety, were prepared using the phosphorylation polycondensation technique. FT-IR and 1↑H NMR... A series of novel polyamides 3a–3d containing 4‐tert‐butyltoluene moiety, were prepared using the phosphorylation polycondensation technique. FT‐IR and 1H NMR... A series of novel polyamides 3a – 3d containing 4‐ tert‐ butyltoluene moiety, were prepared using the phosphorylation polycondensation technique. FT‐IR and 1 H... A series of novel polyamides 3a-3d containing 4-tert-butyltoluene moiety, were prepared using the phosphorylation polycondensation technique. FT-IR and 1H NMR... |
SourceID | proquest crossref wiley istex chongqing |
SourceType | Aggregation Database Index Database Publisher |
StartPage | 2197 |
SubjectTerms | optical transparency Polyamides solubility Solvents Transition temperatures 光学透明性 化学结构 叔丁基 基团 极性溶剂 核磁共振技术 玻璃化转变 聚酰胺薄膜 |
Title | High Glass Transition and Optical Transparency of Novel Organosoluble Polyamides Containing 4-tert-Butyltoluene Moiety |
URI | http://lib.cqvip.com/qk/84126X/201110/39826365.html https://api.istex.fr/ark:/67375/WNG-G551FHNZ-Q/fulltext.pdf https://onlinelibrary.wiley.com/doi/abs/10.1002%2Fcjoc.201180380 https://www.proquest.com/docview/1766806356 |
Volume | 29 |
hasFullText | 1 |
inHoldings | 1 |
isFullTextHit | |
isPrint | |
link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3dbtMwFLamcTFu-EdkG8gXCK6yJXbsxpdQ1laT1gFiouLGsh1nG-visaaIISHxCHvGPcl8nCZbuUECKVKUxFYSH58_6_N3EHpJNReZAJp9LVicca69HfSJq-mppDTeAelQbGJvzEcH2e6ETW7t4m_4IboFN9CMYK9BwZWebd-QhpqvzgQKzjyhOSTtKeVAnv_uI7nJuHqh3hrwDMU8ySYta2NCtpe7A7PCkasOv3l_seSh7sBg_1gKP28HscELDe4j1X5_Az452ZrXesv8_IPa8X9-8AG6twhR8ZtmTj1EK7Z6hNb6bWW4x-gXgEPwEOJuHHxdgH1hVRV4_yysjTe3AdzubTd2JR6773aKw8ZPB7NdTy1-76YX6vS4sDMMHFlNqQqcXf2-BJyCP_nj7by-mNYO6qhYvOcAYPoEHQx2PvVH8aKMQ2yotx-xFYqkJues9J6RM2OztPBmxArKFRGa8aw0RPOsCObEN7WlNoILxkqa5NrSp2i1cpV9hrAwRDElChuY4hTThHLjU7xclCkhJo3QeidGedbQdUgqfApFOYvQ61au3bOGtJlIGGvZjXWEXgWxd83U-QkA4HpMfh4P5dBHmYPR-Iv8EKHNdl7Ihe7PJFBu5gnw_kWIBAH_5XWyv7vf767W_6XTBrpLWnBiuolW6_O5fe6jpVq_CBpxDZ-uDdw |
linkProvider | Wiley-Blackwell |
linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3LbtQwFLVQuygb3oi0BbxAsEqb-DXxEgZmhtJJAbWiYmPZjgO0Q1LaDKJISHwC38iX4OtMUoYNEkiRoiS2Ivv6vqzjcxF6QI2QTALNvpE8ZkIYbwd94moHOimtd0AmFJuY5mJywHYOeYcmhLMwLT9Ev-EGmhHsNSg4bEhvX7CG2qPaBg7OLKGZz9pXmY82IP96-ppc5FyDUHENmIZikbDDjrcxIdvL_YFb4X1dvfvkPcaSj1qF6f6yFID-HsYGPzS6ikw3ghZ-crw1b8yW_foHueN_DfEaurKIUvHjdlldR5dcdQOtDbvicDfRN8CH4DGE3ji4u4D8wroq8N5J2B5vXwO-3ZtvXJc4rz-7GQ5nP2tY8Gbm8Mt6dq4_fijcGQaarLZaBWY_v_8AqIK_-evJvDmfNTWUUnF4WgPG9BY6GD3bH07iRSWH2FJvQmInNUltJnjpnaPg1rG08JbESSo0kYYLVlpiBCuCRfFNXWmsFJLzkiaZcfQ2Wqnqyt1BWFqiuZaFC2RxmhtChfVZXibLlBCbRmi9l6M6aRk7FJU-i6KCR-hRJ9j-W8vbTBTMternOkIPg9z7Zvr0GDBwA67e5GM19oHmaJK_Va8itNktDLVQ_zMFrJtZAtR_ESJBwn_5nRru7A37p_V_6XQfrU32p7tq93n-YgNdJh1WMd1EK83p3N31wVNj7gX1-AV67RH7 |
linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwpV3LbtQwFLVQKwEb3oiUAl4gWKVN_Jp4CQMzQ6FpQVSM2Fi24_DokAxtBlEkJD6Bb-RL8HUmaYcNEkiRoiS2Ivv6vqzjcxG6T42QTALNvpE8ZkIYbwd94moHOimtd0AmFJvYzcXkgO1M-fTMKf6WH6LfcAPNCPYaFHxelNunpKH2Y20DBWeW0Mwn7etM-HACwqJX5DTlGoSCa0A0FIuETTvaxoRsr_YHaoX3dfXus3cYKy5qHWb760r8eTaKDW5odBnpbgAt-uRwa9GYLfvtD27H_xnhFXRpGaPiR-2iuorOueoaujDsSsNdR98BHYLHEHjj4OwC7gvrqsB787A53r4GdLs33rgucV5_cTMcTn7WsNzNzOH9enaiP30o3DEGkqy2VgVmv378BKCCv_nr8aI5mTU1FFJxeLcGhOkNdDB6-no4iZd1HGJLvQGJndQktZngpXeNglvH0sLbESep0EQaLlhpiRGsCPbEN3WlsVJIzkuaZMbRm2itqit3C2FpieZaFi5QxWluCBXW53iZLFNCbBqhjV6Mat7ydSgqfQ5FBY_Qw06u_beWtZkomGvVz3WEHgSx98300SEg4AZcvcnHauzDzNEkf6teRmizWxdqqfzHCjg3swSI_yJEgoD_8js13Nkb9k8b_9LpHjq__2SkXjzLn99GF0kHVEw30VpztHB3fOTUmLtBOX4DOh4Qqg |
openUrl | ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=article&rft.atitle=High+Glass+Transition+and+Optical+Transparency+of+Novel+Organosoluble+Polyamides+Containing+4-tert-Butyltoluene+Moiety&rft.jtitle=%E4%B8%AD%E5%9B%BD%E5%8C%96%E5%AD%A6%EF%BC%9A%E8%8B%B1%E6%96%87%E7%89%88&rft.au=%E6%B1%AA%E7%A7%B0%E6%84%8F+%E8%B5%B5%E6%99%93%E7%87%95+%E6%9D%8E%E5%85%89+%E6%B1%9F%E5%BB%BA%E6%98%8E&rft.date=2011-10-01&rft.issn=1001-604X&rft.eissn=1614-7065&rft.volume=29&rft.issue=10&rft.spage=2197&rft.epage=2201&rft_id=info:doi/10.1002%2Fcjoc.201180380&rft.externalDocID=39826365 |
thumbnail_s | http://utb.summon.serialssolutions.com/2.0.0/image/custom?url=http%3A%2F%2Fimage.cqvip.com%2Fvip1000%2Fqk%2F84126X%2F84126X.jpg |