High-Mobility n‑Type Conjugated Polymers Based on Electron-Deficient Tetraazabenzodifluoranthene Diimide for Organic Electronics
High-mobility p-type and ambipolar conjugated polymers have been widely reported. However, high-mobility n-type conjugated polymers are still rare. Herein we present poly(tetraazabenzodifluoranthene diimide)s, PBFI-T and PBFI-BT, which exhibit a novel two-dimensional (2D) π-conjugation along the mai...
Saved in:
| Published in | Journal of the American Chemical Society Vol. 135; no. 40; pp. 14920 - 14923 |
|---|---|
| Main Authors | , , , |
| Format | Journal Article |
| Language | English |
| Published |
United States
American Chemical Society
09.10.2013
|
| Subjects | |
| Online Access | Get full text |
Cover
Loading…
| Abstract | High-mobility p-type and ambipolar conjugated polymers have been widely reported. However, high-mobility n-type conjugated polymers are still rare. Herein we present poly(tetraazabenzodifluoranthene diimide)s, PBFI-T and PBFI-BT, which exhibit a novel two-dimensional (2D) π-conjugation along the main chain and in the lateral direction, leading to high-mobility unipolar n-channel transport in field-effect transistors. The n-type polymers exhibit electron mobilities of up to 0.30 cm2/(V s), which is among the highest values for unipolar n-type conjugated polymers. Complementary inverters incorporating n-channel PBFI-T transistors produced nearly perfect switching characteristics with a high gain of 107. |
|---|---|
| AbstractList | High-mobility p-type and ambipolar conjugated polymers have been widely reported. However, high-mobility n-type conjugated polymers are still rare. Herein we present poly(tetraazabenzodifluoranthene diimide)s, PBFI-T and PBFI-BT, which exhibit a novel two-dimensional (2D) π-conjugation along the main chain and in the lateral direction, leading to high-mobility unipolar n-channel transport in field-effect transistors. The n-type polymers exhibit electron mobilities of up to 0.30 cm(2)/(V s), which is among the highest values for unipolar n-type conjugated polymers. Complementary inverters incorporating n-channel PBFI-T transistors produced nearly perfect switching characteristics with a high gain of 107.High-mobility p-type and ambipolar conjugated polymers have been widely reported. However, high-mobility n-type conjugated polymers are still rare. Herein we present poly(tetraazabenzodifluoranthene diimide)s, PBFI-T and PBFI-BT, which exhibit a novel two-dimensional (2D) π-conjugation along the main chain and in the lateral direction, leading to high-mobility unipolar n-channel transport in field-effect transistors. The n-type polymers exhibit electron mobilities of up to 0.30 cm(2)/(V s), which is among the highest values for unipolar n-type conjugated polymers. Complementary inverters incorporating n-channel PBFI-T transistors produced nearly perfect switching characteristics with a high gain of 107. High-mobility p-type and ambipolar conjugated polymers have been widely reported. However, high-mobility n-type conjugated polymers are still rare. Herein we present poly(tetraazabenzodifluoranthene diimide)s, PBFI-T and PBFI-BT, which exhibit a novel two-dimensional (2D) π-conjugation along the main chain and in the lateral direction, leading to high-mobility unipolar n-channel transport in field-effect transistors. The n-type polymers exhibit electron mobilities of up to 0.30 cm2/(V s), which is among the highest values for unipolar n-type conjugated polymers. Complementary inverters incorporating n-channel PBFI-T transistors produced nearly perfect switching characteristics with a high gain of 107. High-mobility p-type and ambipolar conjugated polymers have been widely reported. However, high-mobility n-type conjugated polymers are still rare. Herein we present poly(tetraazabenzodifluoranthene diimide)s, PBFI-T and PBFI-BT, which exhibit a novel two-dimensional (2D) π-conjugation along the main chain and in the lateral direction, leading to high-mobility unipolar n-channel transport in field-effect transistors. The n-type polymers exhibit electron mobilities of up to 0.30 cm(2)/(V s), which is among the highest values for unipolar n-type conjugated polymers. Complementary inverters incorporating n-channel PBFI-T transistors produced nearly perfect switching characteristics with a high gain of 107. High-mobility p-type and ambipolar conjugated polymers have been widely reported. However, high-mobility n-type conjugated polymers are still rare. Herein we present poly(tetraazabenzodifluoranthene diimide)s, PBFI-T and PBFI-BT, which exhibit a novel two-dimensional (2D) π-conjugation along the main chain and in the lateral direction, leading to high-mobility unipolar n-channel transport in field-effect transistors. The n-type polymers exhibit electron mobilities of up to 0.30 cm²/(V s), which is among the highest values for unipolar n-type conjugated polymers. Complementary inverters incorporating n-channel PBFI-T transistors produced nearly perfect switching characteristics with a high gain of 107. |
| Author | Ren, Guoqiang Li, Haiyan Jenekhe, Samson A Kim, Felix Sunjoo |
| AuthorAffiliation | Department of Chemistry Department of Chemical Engineering University of Washington |
| AuthorAffiliation_xml | – name: Department of Chemical Engineering – name: Department of Chemistry – name: University of Washington |
| Author_xml | – sequence: 1 givenname: Haiyan surname: Li fullname: Li, Haiyan – sequence: 2 givenname: Felix Sunjoo surname: Kim fullname: Kim, Felix Sunjoo – sequence: 3 givenname: Guoqiang surname: Ren fullname: Ren, Guoqiang – sequence: 4 givenname: Samson A surname: Jenekhe fullname: Jenekhe, Samson A email: jenekhe@u.washington.edu |
| BackLink | https://www.ncbi.nlm.nih.gov/pubmed/24066927$$D View this record in MEDLINE/PubMed |
| BookMark | eNqFkcFu1DAURS1URKeFBT-AskGii1D7xXGcJZ0WilRUFsM6cpznqUeJPdjOYrpC_AG_2C_BaMosUCVWT1c69y7OOyFHzjsk5DWj7xkFdr5RnDa8Yf0zsmA10LJmII7IglIKZSNFdUxOYtzkyEGyF-QYOBWihWZBfl7b9V35xfd2tGlXuIcfv1a7LRZL7zbzWiUciq9-3E0YYnGhYo7eFVcj6hS8Ky_RWG3RpWKFKSh1r3p0936wZpx9UC7docPi0trJDlgYH4rbsFbO6sOE1fEleW7UGPHV4z0l3z5erZbX5c3tp8_LDzelqrhMpdCtAWl6AbKuFZcaoTFSA1NtTYELXjEUWsJQN6YRSvXQSwPciFq2IIa2OiXv9rvb4L_PGFM32ahxHJVDP8cOsp8qm2vgvyjjvOLAGK0y-uYRnfsJh24b7KTCrvurOANne0AHH2NAc0AY7f68rzu8L7Pn_7DaJpWsd9muHZ9svN03lI7dxs_BZYVPcL8BjJ6pjg |
| CitedBy_id | crossref_primary_10_1002_adma_201903104 crossref_primary_10_1039_C7NJ03272B crossref_primary_10_1021_acsapm_0c00772 crossref_primary_10_1109_TNANO_2024_3396505 crossref_primary_10_1088_0268_1242_30_6_064002 crossref_primary_10_1021_acs_chemmater_5b00173 crossref_primary_10_1039_C4TC01201A crossref_primary_10_1002_anie_202316214 crossref_primary_10_1016_j_dyepig_2023_111889 crossref_primary_10_1021_acs_macromol_1c00200 crossref_primary_10_1039_C8TA02175A crossref_primary_10_1002_ange_202307647 crossref_primary_10_1039_D0RA06436J crossref_primary_10_1021_acsami_6b12540 crossref_primary_10_1021_acs_macromol_9b00834 crossref_primary_10_1002_adma_201500577 crossref_primary_10_1039_C5TC00155B crossref_primary_10_1021_acs_orglett_5b03489 crossref_primary_10_1039_D0TC01041C crossref_primary_10_1002_ajoc_202300497 crossref_primary_10_1021_acs_chemmater_6b00154 crossref_primary_10_1016_j_dyepig_2016_07_022 crossref_primary_10_1021_acs_chemmater_8b04819 crossref_primary_10_1038_s41528_023_00267_y crossref_primary_10_1039_C4TC02273D crossref_primary_10_1002_adfm_201801874 crossref_primary_10_1039_C5TA04229A crossref_primary_10_1021_mz500603f crossref_primary_10_1002_adfm_201401822 crossref_primary_10_1002_adma_201305718 crossref_primary_10_1016_j_ccr_2014_10_009 crossref_primary_10_1016_j_orgel_2016_01_015 crossref_primary_10_1002_anie_201711802 crossref_primary_10_1021_acsnano_3c11193 crossref_primary_10_1039_D3NJ05644A crossref_primary_10_1002_adma_201305981 crossref_primary_10_1016_j_molstruc_2024_137606 crossref_primary_10_1021_cr500225d crossref_primary_10_1002_anie_202307647 crossref_primary_10_1021_acs_macromol_8b01020 crossref_primary_10_1002_advs_202002930 crossref_primary_10_1039_C5RA25884G crossref_primary_10_1142_S2010194514603196 crossref_primary_10_1021_acs_joc_6b02214 crossref_primary_10_1039_D1CC02693C crossref_primary_10_1016_j_jechem_2015_11_003 crossref_primary_10_1039_D1MA00716E crossref_primary_10_1021_ja412533d crossref_primary_10_1021_acs_chemmater_8b05353 crossref_primary_10_6023_cjoc202011038 crossref_primary_10_1002_macp_201600606 crossref_primary_10_1002_asia_201501054 crossref_primary_10_1002_aenm_201501727 crossref_primary_10_1021_acs_macromol_6b00185 crossref_primary_10_1016_j_orgel_2016_06_002 crossref_primary_10_1021_acsami_2c22972 crossref_primary_10_1021_acs_chemmater_9b00106 crossref_primary_10_1039_C3PY01598J crossref_primary_10_1039_C7CC09348A crossref_primary_10_1016_j_dyepig_2021_109344 crossref_primary_10_1021_acsami_5b04907 crossref_primary_10_1039_C4RA14072A crossref_primary_10_1021_acsmacrolett_3c00040 crossref_primary_10_1016_j_dyepig_2020_108877 crossref_primary_10_1039_D3RA05647C crossref_primary_10_1039_D3PY01186K crossref_primary_10_2174_2352096516666230816115259 crossref_primary_10_1016_j_tet_2014_04_002 crossref_primary_10_1021_acs_chemmater_0c03975 crossref_primary_10_1016_j_orgel_2019_03_049 crossref_primary_10_1021_acs_macromol_8b01885 crossref_primary_10_1039_D2TC02679A crossref_primary_10_1002_ange_202102708 crossref_primary_10_1002_ange_202307695 crossref_primary_10_1016_j_mtadv_2020_100086 crossref_primary_10_1039_C8TC05740K crossref_primary_10_1103_PhysRevE_100_062205 crossref_primary_10_1039_C4PY01193G crossref_primary_10_1002_adma_201501214 crossref_primary_10_1021_jacs_6b07826 crossref_primary_10_1103_PhysRevE_90_052915 crossref_primary_10_1021_acs_chemmater_6b02007 crossref_primary_10_1002_chem_201402100 crossref_primary_10_1557_mrc_2015_44 crossref_primary_10_1021_acsami_9b13138 crossref_primary_10_1002_ange_201711802 crossref_primary_10_1039_C7QM00169J crossref_primary_10_1039_C4PY00566J crossref_primary_10_1021_acs_macromol_3c00252 crossref_primary_10_1002_adfm_202210846 crossref_primary_10_1039_D1TC02826J crossref_primary_10_3389_fchem_2019_00362 crossref_primary_10_1002_adfm_201602610 crossref_primary_10_1021_jacs_8b02144 crossref_primary_10_1021_ma502042k crossref_primary_10_1021_acs_macromol_6b01446 crossref_primary_10_1002_adfm_201503379 crossref_primary_10_1021_cm500832h crossref_primary_10_1039_D4TC03306J crossref_primary_10_1021_acsami_2c17969 crossref_primary_10_1039_C7TC05900K crossref_primary_10_1103_PhysRevE_109_024207 crossref_primary_10_1002_asia_201501389 crossref_primary_10_1021_acs_chemrev_6b00076 crossref_primary_10_1021_acs_chemmater_7b00056 crossref_primary_10_1039_C8TC04940H crossref_primary_10_1039_C6CC02603F crossref_primary_10_1021_acsami_0c16056 crossref_primary_10_1007_s00289_019_02872_2 crossref_primary_10_1039_D1SC01711J crossref_primary_10_1039_D2CC06626B crossref_primary_10_1021_acsapm_8b00234 crossref_primary_10_1039_C3TC32046D crossref_primary_10_1016_j_dyepig_2015_10_046 crossref_primary_10_1002_adfm_201804839 crossref_primary_10_1002_adfm_202413611 crossref_primary_10_1016_j_orgel_2014_10_026 crossref_primary_10_1016_j_orgel_2016_05_003 crossref_primary_10_1002_anie_202307695 crossref_primary_10_1007_s11426_015_5399_5 crossref_primary_10_1002_anie_202102708 crossref_primary_10_1039_C6RA03221D crossref_primary_10_1021_acsami_9b00531 crossref_primary_10_1039_C7TC01680H crossref_primary_10_1021_ja508807m crossref_primary_10_1021_acs_macromol_6b00540 crossref_primary_10_1002_ange_202316214 crossref_primary_10_1093_nsr_nwv047 crossref_primary_10_1021_ma500626t crossref_primary_10_1039_D1TC02048J crossref_primary_10_1021_ma5003694 crossref_primary_10_1039_C6TA01933A crossref_primary_10_1039_D0TC04962J crossref_primary_10_1002_celc_201600628 crossref_primary_10_1021_acs_orglett_7b03041 crossref_primary_10_1007_s10895_014_1454_4 |
| Cites_doi | 10.1021/cr0501543 10.1039/c1jm12953h 10.1002/anie.201204066 10.1021/cm2034273 10.1021/ma061861g 10.1002/anie.201210085 10.1021/ja403624a 10.1038/nature07727 10.1063/1.126669 10.1021/ja108861q 10.1021/ja201485p 10.1021/cr100380z 10.1039/c0cs00194e 10.1021/cm102419z 10.1021/ja209328m 10.1021/ar200006r 10.1002/adma.200903628 10.1002/adma.200901819 10.1002/adfm.201100592 10.1038/nature05533 10.1021/ma0100448 10.1021/cm049391x 10.1002/aenm.201100215 10.1038/35000530 10.1038/nmat2291 10.1021/ja107678m 10.1002/adma.201290204 10.1021/ja0371810 10.1021/ja802266u 10.1038/44359 |
| ContentType | Journal Article |
| Copyright | Copyright © 2013 American Chemical
Society |
| Copyright_xml | – notice: Copyright © 2013 American Chemical Society |
| DBID | AAYXX CITATION NPM 7X8 7S9 L.6 |
| DOI | 10.1021/ja407471b |
| DatabaseName | CrossRef PubMed MEDLINE - Academic AGRICOLA AGRICOLA - Academic |
| DatabaseTitle | CrossRef PubMed MEDLINE - Academic AGRICOLA AGRICOLA - Academic |
| DatabaseTitleList | MEDLINE - Academic PubMed AGRICOLA |
| Database_xml | – sequence: 1 dbid: NPM name: PubMed url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed sourceTypes: Index Database |
| DeliveryMethod | fulltext_linktorsrc |
| Discipline | Chemistry |
| EISSN | 1520-5126 |
| EndPage | 14923 |
| ExternalDocumentID | 24066927 10_1021_ja407471b f33182062 |
| Genre | Journal Article |
| GroupedDBID | - .K2 02 4.4 53G 55A 5GY 5RE 5VS 7~N 85S AABXI ABFLS ABMVS ABPPZ ABPTK ABUCX ABUFD ACGFS ACJ ACNCT ACS AEESW AENEX AETEA AFEFF ALMA_UNASSIGNED_HOLDINGS AQSVZ BAANH BKOMP CS3 DU5 DZ EBS ED ED~ EJD ET F5P GNL IH9 JG JG~ K2 LG6 P2P ROL RXW TAE TAF TN5 UHB UI2 UKR UPT VF5 VG9 VQA W1F WH7 X XFK YZZ ZHY --- -DZ -ET -~X .DC AAHBH AAYXX ABBLG ABJNI ABLBI ABQRX ACBEA ACGFO ADHLV AGXLV AHDLI AHGAQ CITATION CUPRZ GGK IH2 XSW YQT ZCA ~02 AAYWT NPM 7X8 7S9 L.6 |
| ID | FETCH-LOGICAL-a348t-6c9f28fb62855a48ce27f8c21a950246431e6c82d57f76aab2b8f24f658926d93 |
| IEDL.DBID | ACS |
| ISSN | 0002-7863 1520-5126 |
| IngestDate | Fri Jul 11 13:44:37 EDT 2025 Mon Jul 21 09:48:37 EDT 2025 Mon Jul 21 06:04:41 EDT 2025 Thu Apr 24 22:57:16 EDT 2025 Tue Jul 01 04:32:49 EDT 2025 Thu Aug 27 13:42:12 EDT 2020 |
| IsPeerReviewed | true |
| IsScholarly | true |
| Issue | 40 |
| Language | English |
| LinkModel | DirectLink |
| MergedId | FETCHMERGED-LOGICAL-a348t-6c9f28fb62855a48ce27f8c21a950246431e6c82d57f76aab2b8f24f658926d93 |
| Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
| PMID | 24066927 |
| PQID | 1443421103 |
| PQPubID | 23479 |
| PageCount | 4 |
| ParticipantIDs | proquest_miscellaneous_2000351272 proquest_miscellaneous_1443421103 pubmed_primary_24066927 crossref_primary_10_1021_ja407471b crossref_citationtrail_10_1021_ja407471b acs_journals_10_1021_ja407471b |
| ProviderPackageCode | JG~ 55A AABXI GNL VF5 7~N ACJ VG9 W1F ACS AEESW AFEFF .K2 ABMVS ABUCX IH9 BAANH AQSVZ ED~ UI2 CITATION AAYXX |
| PublicationCentury | 2000 |
| PublicationDate | 20131009 2013-10-09 2013-Oct-09 |
| PublicationDateYYYYMMDD | 2013-10-09 |
| PublicationDate_xml | – month: 10 year: 2013 text: 20131009 day: 09 |
| PublicationDecade | 2010 |
| PublicationPlace | United States |
| PublicationPlace_xml | – name: United States |
| PublicationTitle | Journal of the American Chemical Society |
| PublicationTitleAlternate | J. Am. Chem. Soc |
| PublicationYear | 2013 |
| Publisher | American Chemical Society |
| Publisher_xml | – name: American Chemical Society |
| References | Meijer E. J. (ref10/cit10b) 2000; 76 Zaumseil J. (ref1/cit1a) 2007; 107 Lee J.-K. (ref4/cit4e) 2011; 133 Wang C. (ref2/cit2a) 2012; 112 Sirringhaus H. (ref10/cit10c) 1999; 401 Facchetti A. (ref1/cit1b) 2011; 23 Lei T. (ref4/cit4f) 2013; 135 Takeda Y. (ref4/cit4d) 2012; 51 Zhu Y. (ref7/cit7) 2006; 39 Li H. (ref6/cit6) 2013; 52 Kim F. S. (ref5/cit5a) 2010; 22 Subramaniyan S. (ref11/cit11) 2011; 1 Usta H. (ref2/cit2b) 2011; 44 Newman C. R. (ref1/cit1c) 2004; 16 Jenekhe S. A. (ref8/cit8) 2001; 34 Mei J. (ref9/cit9) 2011; 133 Caironi M. (ref10/cit10a) 2011; 21 Chen H. (ref3/cit3c) 2012; 24 Briseno A. L. (ref2/cit2f) 2011; 21 Zhao X. (ref2/cit2g) 2011; 40 Yan H. (ref4/cit4b) 2009; 457 Klauk H. (ref2/cit2c) 2007; 445 Crone B. (ref2/cit2d) 2000; 403 Li J. (ref3/cit3a) 2012 Guo X. (ref5/cit5b) 2012; 24 Anthony J. E. (ref2/cit2e) 2010; 22 Guo X. (ref4/cit4c) 2011; 133 Cho J. H. (ref12/cit12) 2008; 7 Usta H. (ref5/cit5c) 2008; 130 Tsao H. N. (ref3/cit3b) 2011; 133 Babel A. (ref4/cit4a) 2003; 125 |
| References_xml | – volume: 107 start-page: 1296 year: 2007 ident: ref1/cit1a publication-title: Chem. Rev. doi: 10.1021/cr0501543 – volume: 21 start-page: 16461 year: 2011 ident: ref2/cit2f publication-title: J. Mater. Chem. doi: 10.1039/c1jm12953h – volume: 51 start-page: 9042 year: 2012 ident: ref4/cit4d publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201204066 – start-page: 2 year: 2012 ident: ref3/cit3a publication-title: Sci. Rep. – volume: 24 start-page: 1434 year: 2012 ident: ref5/cit5b publication-title: Chem. Mater. doi: 10.1021/cm2034273 – volume: 39 start-page: 8712 year: 2006 ident: ref7/cit7 publication-title: Macromolecules doi: 10.1021/ma061861g – volume: 52 start-page: 5513 year: 2013 ident: ref6/cit6 publication-title: Angew. Chem., Int. Ed. doi: 10.1002/anie.201210085 – volume: 135 start-page: 12168 year: 2013 ident: ref4/cit4f publication-title: J. Am. Chem. Soc. doi: 10.1021/ja403624a – volume: 457 start-page: 679 year: 2009 ident: ref4/cit4b publication-title: Nature doi: 10.1038/nature07727 – volume: 76 start-page: 3433 year: 2000 ident: ref10/cit10b publication-title: Appl. Phys. Lett. doi: 10.1063/1.126669 – volume: 133 start-page: 2605 year: 2011 ident: ref3/cit3b publication-title: J. Am. Chem. Soc. doi: 10.1021/ja108861q – volume: 133 start-page: 9949 year: 2011 ident: ref4/cit4e publication-title: J. Am. Chem. Soc. doi: 10.1021/ja201485p – volume: 112 start-page: 2208 year: 2012 ident: ref2/cit2a publication-title: Chem. Rev. doi: 10.1021/cr100380z – volume: 40 start-page: 3728 year: 2011 ident: ref2/cit2g publication-title: Chem. Soc. Rev. doi: 10.1039/c0cs00194e – volume: 23 start-page: 733 year: 2011 ident: ref1/cit1b publication-title: Chem. Mater. doi: 10.1021/cm102419z – volume: 133 start-page: 20130 year: 2011 ident: ref9/cit9 publication-title: J. Am. Chem. Soc. doi: 10.1021/ja209328m – volume: 44 start-page: 501 year: 2011 ident: ref2/cit2b publication-title: Acc. Chem. Res. doi: 10.1021/ar200006r – volume: 22 start-page: 3876 year: 2010 ident: ref2/cit2e publication-title: Adv. Mater. doi: 10.1002/adma.200903628 – volume: 22 start-page: 478 year: 2010 ident: ref5/cit5a publication-title: Adv. Mater. doi: 10.1002/adma.200901819 – volume: 21 start-page: 3371 year: 2011 ident: ref10/cit10a publication-title: Adv. Funct. Mater. doi: 10.1002/adfm.201100592 – volume: 445 start-page: 745 year: 2007 ident: ref2/cit2c publication-title: Nature doi: 10.1038/nature05533 – volume: 34 start-page: 7315 year: 2001 ident: ref8/cit8 publication-title: Macromolecules doi: 10.1021/ma0100448 – volume: 16 start-page: 4436 year: 2004 ident: ref1/cit1c publication-title: Chem. Mater. doi: 10.1021/cm049391x – volume: 1 start-page: 854 year: 2011 ident: ref11/cit11 publication-title: Adv. Energy Mater. doi: 10.1002/aenm.201100215 – volume: 403 start-page: 521 year: 2000 ident: ref2/cit2d publication-title: Nature doi: 10.1038/35000530 – volume: 7 start-page: 900 year: 2008 ident: ref12/cit12 publication-title: Nat. Mater. doi: 10.1038/nmat2291 – volume: 133 start-page: 1405 year: 2011 ident: ref4/cit4c publication-title: J. Am. Chem. Soc. doi: 10.1021/ja107678m – volume: 24 start-page: 4589 year: 2012 ident: ref3/cit3c publication-title: Adv. Mater. doi: 10.1002/adma.201290204 – volume: 125 start-page: 13656 year: 2003 ident: ref4/cit4a publication-title: J. Am. Chem. Soc. doi: 10.1021/ja0371810 – volume: 130 start-page: 8580 year: 2008 ident: ref5/cit5c publication-title: J. Am. Chem. Soc. doi: 10.1021/ja802266u – volume: 401 start-page: 685 year: 1999 ident: ref10/cit10c publication-title: Nature doi: 10.1038/44359 |
| SSID | ssj0004281 |
| Score | 2.4779484 |
| Snippet | High-mobility p-type and ambipolar conjugated polymers have been widely reported. However, high-mobility n-type conjugated polymers are still rare. Herein we... |
| SourceID | proquest pubmed crossref acs |
| SourceType | Aggregation Database Index Database Enrichment Source Publisher |
| StartPage | 14920 |
| SubjectTerms | electronics polymers |
| Title | High-Mobility n‑Type Conjugated Polymers Based on Electron-Deficient Tetraazabenzodifluoranthene Diimide for Organic Electronics |
| URI | http://dx.doi.org/10.1021/ja407471b https://www.ncbi.nlm.nih.gov/pubmed/24066927 https://www.proquest.com/docview/1443421103 https://www.proquest.com/docview/2000351272 |
| Volume | 135 |
| hasFullText | 1 |
| inHoldings | 1 |
| isFullTextHit | |
| isPrint | |
| link | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwhV1Lb9QwELZKOcClvOnyqMzjwMXVZuzEyRF2W1VIICRaqbeVX5FSFgd1k0N7QvwD_iK_hJk8FhBduE_sJB7r--yZ-Yaxl1OHXmFkIiyiv1BWToXRqRJB2RIRXikVOrXP99nRiXp7mp5usRcbIvhA-kCKRN4Te41dhww3L_Gf2cdfxY-QJyPH1XkmR_mg3x8l6HGrP6FnA5_scOXwFpuP1Tl9Osmn_bax--7yb7HGf73ybbYz8Er-uneEO2wrxLvsxmxs53aPfaOMDvGu7pJhL3j88fU7nUH5rI5nLd2lef6hXl7QNTZ_g9DmeR35wdAkR8wDKU0gQPHj0JwbQ6lg8bL2Vbls0YkiaSgEPq-qz5UPHIkw74s83XqIyq3us5PDg-PZkRgaMAgjVd6IzBUl5KWlMsvUqNwF0GXuIDFFitiOZCYJmcvBp7rUmTEWbF6CKpHVFJD5Qj5g27GOYZfxRKUyaC9xJFCpn1qLVM5NnSwS4zT4CdvDFVoMG2i16GLjgGeT8VdO2Ktx8RZukC-nLhrLq0yfr02_9JodVxk9Gz1ggStBYRITQ93i1EpJRediudkG-hAsaJiwh737rKcijpQVoB_975Mes5tAzTUoHaF4wrab8zY8RYrT2L3OxX8C4jb1UA |
| linkProvider | American Chemical Society |
| linkToHtml | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1Lb9QwELagHMqF8ixboBjEgYurje3EybFsWy3QVkhspd4ivyIFFgc1yaE9If4Bf5FfwkweW0Ct4D6xnXii77Nn5htCXk0teIUWETOA_kwaMWVaxZJ5aQpAeCml79Q-j5P5iXx3Gp8OMjlYCwOLqGGkugviX6oLoEyQRK33yNwkt4CEcPTm3dnHyxpInkYj1VVpIkYVod8fRQSy9Z8IdA2t7ODlYKPvU9QtrMsq-bzTNmbHXvyl2fh_K79L7gwsk-72bnGP3PDhPlmfjc3dHpDvmN_BjqouNfachp_ffuCJlM6q8KnFmzVHP1TLc7zUpm8A6BytAt0fWuawPY-6EwBXdOGbM60xMSxcVK4sli24VEBFBU_3yvJL6TwFWkz7kk-7GqK09UNycrC_mM3Z0I6BaSHThiU2K3haGCy6jLVMreeqSC2PdBYD0gO1iXxiU-5iVahEa8NNWnBZAMfJeOIy8YishSr4x4RGMhZeOQEjcRm7qTFA7OzUiizSVnE3IdvwJfPhd6rzLlLO4aQyfsoJeT3uYW4HMXPsqbG8yvTlyvRrr-BxldGL0RFy2AkMmujgqxamllJIPCWL6214H5Dlik_IZu9Fq6mQMSUZV1v_eqXnZH2-ODrMD98ev39CbnNsu4GJCtlTstactf4ZkJ_GbHde_wu6Cv2x |
| linkToPdf | http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1Lb9QwELagSNAL75blUQziwMXVxnbi5Fh2uyqvUolW6i3yK1JgcaomObQnxD_gL_JLmMljeagV3Ce2Y48133hmviHkxdSCVmgRMQPWn0kjpkyrWDIvTQEWXkrpO7bP_WTvSL45jo8HRxFrYWARNYxUd0F8vNUnrhgYBpAqSCLfe2SukmsYrkON3pl9_FUHydNohLsqTcTIJPT7p2iFbP2nFboEWnYmZnGLfFgtrsss-bzdNmbbnv_F2_j_q79Nbg5ok-706nGHXPHhLrkxG5u83SPfMM-Dva-6FNkzGn58_Y6eKZ1V4VOLL2yOHlTLM3zcpq_A4DlaBbo7tM5hc4_8E2C26KFvTrXGBLFwXrmyWLagWgGZFTydl-WX0nkK8Jj2pZ92NURp6_vkaLF7ONtjQ1sGpoVMG5bYrOBpYbD4MtYytZ6rIrU80lkMFh8gTuQTm3IXq0IlWhtu0oLLArBOxhOXiQ2yFqrgHxAayVh45QSMxGXspsYAwLNTK7JIW8XdhGzBbubDtarzLmLOwWMZt3JCXo7nmNuB1Bx7aywvEn2-Ej3pmTwuEno2KkMOJ4HBEx181cLUUgqJ3rK4XIb3gVmu-IRs9pq0mgqRU5Jx9fBfv_SUXD-YL_J3r_ffPiLrHLtvYL5C9pisNaetfwIYqDFbneL_BPoWAEM |
| 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-mobility+n-type+conjugated+polymers+based+on+electron-deficient+tetraazabenzodifluoranthene+diimide+for+organic+electronics&rft.jtitle=Journal+of+the+American+Chemical+Society&rft.au=Li%2C+Haiyan&rft.au=Kim%2C+Felix+Sunjoo&rft.au=Ren%2C+Guoqiang&rft.au=Jenekhe%2C+Samson+A&rft.date=2013-10-09&rft.eissn=1520-5126&rft.volume=135&rft.issue=40&rft.spage=14920&rft_id=info:doi/10.1021%2Fja407471b&rft_id=info%3Apmid%2F24066927&rft.externalDocID=24066927 |
| thumbnail_l | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0002-7863&client=summon |
| thumbnail_m | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0002-7863&client=summon |
| thumbnail_s | http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0002-7863&client=summon |