Combination of RAFT and Pd(II)-Initiated Isocyanide Polymerizations: A Versatile Method for Facile Synthesis of Helical Poly(phenyl isocyanide) Block and Star Copolymers

We report a new method for facile synthesis of block and star copolymers composed of helical poly­(phenyl isocyanide) and polyacrylate segments via combination of Pd­(II)-initiated isocyanide polymerization and reversible addition–fragmentation chain transfer (RAFT) controlled radical polymerization...

Full description

Saved in:
Bibliographic Details
Published inMacromolecules Vol. 51; no. 3; pp. 737 - 745
Main Authors Jiang, Zhi-Qiang, Zhao, Song-Qing, Su, Yi-Xu, Liu, Na, Wu, Zong-Quan
Format Journal Article
LanguageEnglish
Published American Chemical Society 13.02.2018
Online AccessGet full text

Cover

Loading…
Abstract We report a new method for facile synthesis of block and star copolymers composed of helical poly­(phenyl isocyanide) and polyacrylate segments via combination of Pd­(II)-initiated isocyanide polymerization and reversible addition–fragmentation chain transfer (RAFT) controlled radical polymerization. First, an alkyne–Pd­(II) complex containing benzyl trithiocarbonate substituent was designed and synthesized. The Pd­(II) moiety of the complex can catalyzed the living polymerization of phenyl isocyanides, while the benzyl trithiocarbonate unit can be used as a chain transfer agent for RAFT polymerization. Upon combination of the two living polymerizations, a series of block copolymers containing poly­(phenyl isocyanide) and polyacrylate, poly­(aryl vinyl) blocks with expected molecular weights (M ns) and narrow molecular weight distributions (M w/M ns) can be facilely prepared under controlled manner. Some of these block copolymers exhibited interesting self-assembly and stimuli-responsive properties. Taking advantage of this synthetic approach, core cross-linked star block copolymer carrying polyacrylate-block-polyisocyanide arms can be readily prepared through the copolymerization with a cross-linker, ethylene glycol dimethacrylate. Moreover, miktoarm star copolymers carrying helical polyisocyanides and polyacrylates arms can also be prepared under controlled manner.
AbstractList We report a new method for facile synthesis of block and star copolymers composed of helical poly­(phenyl isocyanide) and polyacrylate segments via combination of Pd­(II)-initiated isocyanide polymerization and reversible addition–fragmentation chain transfer (RAFT) controlled radical polymerization. First, an alkyne–Pd­(II) complex containing benzyl trithiocarbonate substituent was designed and synthesized. The Pd­(II) moiety of the complex can catalyzed the living polymerization of phenyl isocyanides, while the benzyl trithiocarbonate unit can be used as a chain transfer agent for RAFT polymerization. Upon combination of the two living polymerizations, a series of block copolymers containing poly­(phenyl isocyanide) and polyacrylate, poly­(aryl vinyl) blocks with expected molecular weights (M ns) and narrow molecular weight distributions (M w/M ns) can be facilely prepared under controlled manner. Some of these block copolymers exhibited interesting self-assembly and stimuli-responsive properties. Taking advantage of this synthetic approach, core cross-linked star block copolymer carrying polyacrylate-block-polyisocyanide arms can be readily prepared through the copolymerization with a cross-linker, ethylene glycol dimethacrylate. Moreover, miktoarm star copolymers carrying helical polyisocyanides and polyacrylates arms can also be prepared under controlled manner.
Author Zhao, Song-Qing
Su, Yi-Xu
Wu, Zong-Quan
Liu, Na
Jiang, Zhi-Qiang
AuthorAffiliation Department of Polymer Science and Engineering, School of Chemistry and Chemical Engineering, and Anhui Key Laboratory of Advanced Catalytic Materials and Reaction Engineering
AuthorAffiliation_xml – name: Department of Polymer Science and Engineering, School of Chemistry and Chemical Engineering, and Anhui Key Laboratory of Advanced Catalytic Materials and Reaction Engineering
Author_xml – sequence: 1
  givenname: Zhi-Qiang
  surname: Jiang
  fullname: Jiang, Zhi-Qiang
– sequence: 2
  givenname: Song-Qing
  surname: Zhao
  fullname: Zhao, Song-Qing
– sequence: 3
  givenname: Yi-Xu
  surname: Su
  fullname: Su, Yi-Xu
– sequence: 4
  givenname: Na
  surname: Liu
  fullname: Liu, Na
– sequence: 5
  givenname: Zong-Quan
  orcidid: 0000-0001-6657-9316
  surname: Wu
  fullname: Wu, Zong-Quan
  email: zqwu@hfut.edu.cn
BookMark eNp9kL1OwzAQxy1UJNrCGzB4hCHFHzFJ2EpFIRKIigJrZMcX1ZDYlR2G8Ea8JUkLjEynu9P_Q78JGllnAaFTSmaUMHohyzBrZOld4-pZogi7vOQHaEwFI5FIuRihMSEsjjKWJUdoEsIbIZSKmI_R18I1yljZGmexq_DTfPmMpdV4pc_y_DzKrWmNbEHjPLiyk9ZowCtXdw1487mThSs8x6_gQ7_VgB-g3TiNK-fxUpbDZd3ZdgPBhCHgDmpTynrncbbdgO1qbP6sz_F17cr3XYN1Kz1euO0-LByjw0rWAU5-5hS9LG-eF3fR_eNtvpjfR5KLtI2gSiGjiRaKM0iJVlkaS6JAJUwA03FJWZqlWZXEHKoyJooA5xnnSqgk4anmUxTvfXueIXioiq03jfRdQUkx4C563MUv7uIHdy8je9nwfXMf3vYl_5d8Ax9Vi94
CitedBy_id crossref_primary_10_1002_anie_202014813
crossref_primary_10_1021_acs_macromol_8b01361
crossref_primary_10_1021_acs_macromol_8b01282
crossref_primary_10_1021_acsmacrolett_2c00212
crossref_primary_10_1039_C8PY00865E
crossref_primary_10_1002_anie_202011661
crossref_primary_10_1002_macp_201800574
crossref_primary_10_1002_pol_20210345
crossref_primary_10_1021_acs_macromol_2c01943
crossref_primary_10_1039_D0PY01558J
crossref_primary_10_1016_j_ccr_2018_06_017
crossref_primary_10_1021_acs_macromol_8b02008
crossref_primary_10_1021_acs_macromol_8b01478
crossref_primary_10_1002_ange_202011661
crossref_primary_10_1002_marc_202100029
crossref_primary_10_1002_ange_202014813
crossref_primary_10_3390_polym10030318
crossref_primary_10_1021_acs_langmuir_9b02194
crossref_primary_10_1002_chir_23387
crossref_primary_10_1002_app_49408
crossref_primary_10_1016_j_eurpolymj_2019_05_054
crossref_primary_10_1016_j_eurpolymj_2021_110318
crossref_primary_10_1039_C9PY00248K
crossref_primary_10_3390_polym11081360
crossref_primary_10_1021_jacs_9b03177
crossref_primary_10_1007_s10853_018_2448_4
crossref_primary_10_1039_C9NR07816A
crossref_primary_10_1021_acs_accounts_1c00489
crossref_primary_10_1039_C9PY01656B
crossref_primary_10_1080_10601325_2019_1691452
crossref_primary_10_1002_ijch_201800023
crossref_primary_10_1016_j_colsurfa_2022_128680
crossref_primary_10_1016_j_polymer_2021_123431
crossref_primary_10_1021_acs_macromol_2c02490
crossref_primary_10_1021_acs_macromol_9b00306
crossref_primary_10_1007_s11164_019_03965_3
crossref_primary_10_1002_pol_20220520
crossref_primary_10_1021_acs_macromol_2c00826
crossref_primary_10_1002_marc_202000463
crossref_primary_10_1039_C9RA10430E
crossref_primary_10_1002_marc_202300005
crossref_primary_10_1039_D1SC05361B
crossref_primary_10_1021_acs_langmuir_9b01241
crossref_primary_10_1021_acs_macromol_8b01179
crossref_primary_10_1021_acs_macromol_9b02118
crossref_primary_10_6023_cjoc202305003
crossref_primary_10_1016_j_eurpolymj_2019_05_035
crossref_primary_10_1002_macp_202000362
crossref_primary_10_1039_D0NA00127A
Cites_doi 10.1021/bc200240q
10.1039/c1py00360g
10.1021/ja056841t
10.1021/ie070357c
10.1021/acs.macromol.5b00407
10.1039/C7PY00028F
10.1038/nchem.2634
10.1021/ja711283c
10.1021/acs.macromol.6b02403
10.1021/mz300309c
10.1021/acsmacrolett.6b00267
10.1021/acs.orglett.5b00780
10.1021/ma901701w
10.1021/acs.macromol.5b02142
10.1021/jacs.6b10624
10.1021/mz200161s
10.1021/acsmacrolett.7b00529
10.1126/science.1103350
10.1021/ol301723e
10.1021/ja502843f
10.1021/ma502283f
10.1021/ar800086w
10.1021/acs.macromol.7b01453
10.1039/C7PY01062A
10.1016/j.biomaterials.2011.05.049
10.1021/acs.chemrev.6b00008
10.1002/anie.201101381
10.1073/pnas.37.4.205
10.1021/acsmacrolett.5b00530
10.1021/acs.macromol.6b02060
10.1021/acs.macromol.7b01028
10.1021/acs.macromol.5b02223
10.1021/acs.macromol.5b00811
10.1021/ja070956a
10.1039/c3py00708a
10.1021/acs.macromol.6b02558
10.1021/acsmacrolett.6b00191
10.1021/ma302536t
10.1021/acs.chemrev.6b00354
10.1021/acsmacrolett.7b00439
10.1021/acsmacrolett.7b00857
10.1039/C2PY20612A
10.1021/acs.macromol.6b01870
10.1021/acs.macromol.6b01378
10.1038/171737a0
10.1021/ma8023552
10.1021/acsmacrolett.7b00583
10.1039/C0PY00246A
10.1021/ma4015802
10.1021/ja5004747
10.1039/c2cc31406a
10.1021/ja4098803
10.1021/bm2005164
10.1021/acsmacrolett.5b00108
10.1038/nature11839
10.1021/acsmacrolett.6b00818
10.1021/ja900036n
ContentType Journal Article
Copyright Copyright © 2018 American Chemical Society
Copyright_xml – notice: Copyright © 2018 American Chemical Society
DBID AAYXX
CITATION
DOI 10.1021/acs.macromol.7b02663
DatabaseName CrossRef
DatabaseTitle CrossRef
DatabaseTitleList
DeliveryMethod fulltext_linktorsrc
Discipline Chemistry
EISSN 1520-5835
EndPage 745
ExternalDocumentID 10_1021_acs_macromol_7b02663
b203896970
GroupedDBID .K2
53G
55A
5GY
5VS
7~N
AABXI
ABFLS
ABMVS
ABPPZ
ABPTK
ABUCX
ACGFS
ACJ
ACNCT
ACS
AEESW
AENEX
AFEFF
ALMA_UNASSIGNED_HOLDINGS
AQSVZ
BAANH
CS3
DU5
EBS
ED
ED~
EJD
F5P
GNL
IH9
IHE
JG
JG~
K2
LG6
P2P
ROL
TN5
TWZ
UI2
VF5
VG9
W1F
WH7
X
YZZ
-~X
4.4
AAHBH
AAYXX
ABJNI
ABQRX
ACBEA
ACGFO
ADHLV
AGXLV
AHGAQ
CITATION
CUPRZ
GGK
ID FETCH-LOGICAL-a358t-ef8e917d5b32e80db984a0beb725e2d4c128989f743efc40b0e33933b5b7738d3
IEDL.DBID ACS
ISSN 0024-9297
IngestDate Fri Aug 23 02:20:01 EDT 2024
Fri Feb 05 20:53:48 EST 2021
IsPeerReviewed true
IsScholarly true
Issue 3
Language English
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-a358t-ef8e917d5b32e80db984a0beb725e2d4c128989f743efc40b0e33933b5b7738d3
ORCID 0000-0001-6657-9316
PageCount 9
ParticipantIDs crossref_primary_10_1021_acs_macromol_7b02663
acs_journals_10_1021_acs_macromol_7b02663
ProviderPackageCode JG~
55A
AABXI
GNL
VF5
7~N
ACJ
VG9
W1F
ACS
AEESW
AFEFF
.K2
ABMVS
ABUCX
IH9
BAANH
AQSVZ
ED~
UI2
PublicationCentury 2000
PublicationDate 2018-02-13
PublicationDateYYYYMMDD 2018-02-13
PublicationDate_xml – month: 02
  year: 2018
  text: 2018-02-13
  day: 13
PublicationDecade 2010
PublicationTitle Macromolecules
PublicationTitleAlternate Macromolecules
PublicationYear 2018
Publisher American Chemical Society
Publisher_xml – name: American Chemical Society
References ref9/cit9
ref45/cit45
ref3/cit3
ref27/cit27
ref56/cit56
ref16/cit16
ref52/cit52
ref23/cit23
ref8/cit8
ref31/cit31
ref2/cit2
ref34/cit34
ref37/cit37
ref20/cit20
ref48/cit48
ref17/cit17
ref10/cit10
ref35/cit35
ref53/cit53
ref19/cit19
ref21/cit21
ref42/cit42
ref46/cit46
ref49/cit49
ref13/cit13
ref24/cit24
ref38/cit38
ref50/cit50
ref54/cit54
ref6/cit6
ref36/cit36
ref18/cit18
ref11/cit11
ref25/cit25
ref29/cit29
ref32/cit32
ref39/cit39
ref14/cit14
ref57/cit57
ref5/cit5
ref51/cit51
ref43/cit43
ref28/cit28
ref40/cit40
ref26/cit26
ref55/cit55
ref12/cit12
ref15/cit15
ref41/cit41
ref22/cit22
ref33/cit33
ref4/cit4
ref30/cit30
ref47/cit47
ref1/cit1
ref44/cit44
ref7/cit7
References_xml – ident: ref47/cit47
  doi: 10.1021/bc200240q
– ident: ref45/cit45
  doi: 10.1039/c1py00360g
– ident: ref40/cit40
  doi: 10.1021/ja056841t
– ident: ref27/cit27
  doi: 10.1021/ie070357c
– ident: ref52/cit52
  doi: 10.1021/acs.macromol.5b00407
– ident: ref10/cit10
  doi: 10.1039/C7PY00028F
– ident: ref31/cit31
  doi: 10.1038/nchem.2634
– ident: ref14/cit14
  doi: 10.1021/ja711283c
– ident: ref41/cit41
  doi: 10.1021/acs.macromol.6b02403
– ident: ref7/cit7
  doi: 10.1021/mz300309c
– ident: ref29/cit29
  doi: 10.1021/acsmacrolett.6b00267
– ident: ref56/cit56
  doi: 10.1021/acs.orglett.5b00780
– ident: ref48/cit48
  doi: 10.1021/ma901701w
– ident: ref6/cit6
  doi: 10.1021/acs.macromol.5b02142
– ident: ref51/cit51
  doi: 10.1021/jacs.6b10624
– ident: ref20/cit20
  doi: 10.1021/mz200161s
– ident: ref46/cit46
  doi: 10.1021/acsmacrolett.7b00529
– ident: ref39/cit39
  doi: 10.1126/science.1103350
– ident: ref57/cit57
  doi: 10.1021/ol301723e
– ident: ref26/cit26
  doi: 10.1021/ja502843f
– ident: ref38/cit38
  doi: 10.1021/ma502283f
– ident: ref3/cit3
  doi: 10.1021/ar800086w
– ident: ref32/cit32
  doi: 10.1021/acs.macromol.7b01453
– ident: ref33/cit33
  doi: 10.1039/C7PY01062A
– ident: ref55/cit55
  doi: 10.1016/j.biomaterials.2011.05.049
– ident: ref50/cit50
  doi: 10.1021/acs.chemrev.6b00008
– ident: ref43/cit43
  doi: 10.1002/anie.201101381
– ident: ref1/cit1
  doi: 10.1073/pnas.37.4.205
– ident: ref24/cit24
  doi: 10.1021/acsmacrolett.5b00530
– ident: ref36/cit36
  doi: 10.1021/acs.macromol.6b02060
– ident: ref9/cit9
  doi: 10.1021/acs.macromol.7b01028
– ident: ref44/cit44
  doi: 10.1021/acs.macromol.5b02223
– ident: ref11/cit11
  doi: 10.1021/acs.macromol.5b00811
– ident: ref28/cit28
  doi: 10.1021/ja070956a
– ident: ref22/cit22
  doi: 10.1039/c3py00708a
– ident: ref21/cit21
  doi: 10.1021/acs.macromol.6b02558
– ident: ref19/cit19
  doi: 10.1021/acsmacrolett.6b00191
– ident: ref17/cit17
  doi: 10.1021/ma302536t
– ident: ref4/cit4
  doi: 10.1021/acs.chemrev.6b00354
– ident: ref23/cit23
  doi: 10.1021/acsmacrolett.7b00439
– ident: ref35/cit35
  doi: 10.1021/acsmacrolett.7b00857
– ident: ref25/cit25
  doi: 10.1039/C2PY20612A
– ident: ref12/cit12
  doi: 10.1021/acs.macromol.6b01870
– ident: ref54/cit54
  doi: 10.1021/acs.macromol.6b01378
– ident: ref2/cit2
  doi: 10.1038/171737a0
– ident: ref8/cit8
  doi: 10.1021/ma8023552
– ident: ref30/cit30
  doi: 10.1021/acsmacrolett.7b00583
– ident: ref15/cit15
  doi: 10.1039/C0PY00246A
– ident: ref13/cit13
  doi: 10.1021/ma4015802
– ident: ref37/cit37
  doi: 10.1021/ja5004747
– ident: ref42/cit42
  doi: 10.1039/c2cc31406a
– ident: ref5/cit5
  doi: 10.1021/ja4098803
– ident: ref49/cit49
  doi: 10.1021/bm2005164
– ident: ref53/cit53
  doi: 10.1021/acsmacrolett.5b00108
– ident: ref16/cit16
  doi: 10.1038/nature11839
– ident: ref34/cit34
  doi: 10.1021/acsmacrolett.6b00818
– ident: ref18/cit18
  doi: 10.1021/ja900036n
SSID ssj0011543
Score 2.4977026
Snippet We report a new method for facile synthesis of block and star copolymers composed of helical poly­(phenyl isocyanide) and polyacrylate segments via combination...
SourceID crossref
acs
SourceType Aggregation Database
Publisher
StartPage 737
Title Combination of RAFT and Pd(II)-Initiated Isocyanide Polymerizations: A Versatile Method for Facile Synthesis of Helical Poly(phenyl isocyanide) Block and Star Copolymers
URI http://dx.doi.org/10.1021/acs.macromol.7b02663
Volume 51
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV1Lb9swDBa27LBd1nYP9A0demgOyhRJtqTesmBBU6BbsbZAbwZlyUCQ1Bnq5JD-o_3LUY7dFRs2tEcLBiWIlL-PJikScsShb3OvJdMm9Uw5mTBQiWMc0GcG7kXqYjXy-df09Fqd3SQ3vx3FPyP4ov8J8qp3C3Vy2qynHfoMqXxJXgmN5yNSoeHlQ9QA6cA6oiwUQ9jXbancP6REQMqrR4D0CFlGG-RbW5-zTiiZ9pYL18vv_76u8YmL3iRvG5JJB2ur2CIvQvmOvB62vd3ek5_4GUCXuNYKnRf0-2B0RaH09MIfj8ddNo4pRchCPR2j9lZQTnygF_PZKsZ3msLNEzqg8W8bPs0CPa87UVOkwHQEeRy5XJVILqtJFSdAdIvWUMs4jmllqxmdPIju0s-IqdN6Bch-7-gwtm6Ik1UfyPXoy9XwlDVNGxjIxCxYKExAF9AnTopguHfWKOAuOC2SILzKERCtsQUyl1DkijsepLRSusRpLY2XH0mnnJdhm1CXcOWtAZtrUFBwSKN7hgRLBGsBxA7p4j5nzaGrsjqeLvpZHGw3P2s2f4ewVsvZj_U9Hv99f_cZsvfIG6RRJuZy9-U-6SzuluEAqcrCHdb2-QusWOf8
link.rule.ids 315,783,787,2772,27088,27936,27937,57066,57116
linkProvider American Chemical Society
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwlV1NTxsxELUoPdBLS1uq0vLhQw_k4NRZ22ubW4iIsi1BqATEbWWvvVJEuqnYcEj_Uf9lx85uiiqBxHGt1Xjksfe92ZnxIPSFmp4unGREqtQRbpkghgtLqAGf2VCXpDZUI4_P09EV_3YjbjaQaGthQIkaJNUxiP_vdoHe1zD208QctVlXWnAdUvYCvRQSMDMwosHlOngArGAVWE44AfSXbcXcI1ICLhX1A1x6ADDDN-h6rVrMK7nt3i9st_j9362Nz9Z9G71uKCfur_bIW7Thq3doa9B2enuP_sBHARzkaCM8L_GP_nCCTeXwhTvKsg7JQoIRcFKHM7Dl0lRT5_HFfLYM0Z6mjPMY93H49wZPM4_HsS81BkKMh6YII5fLCqhmPa3DBIB1YW9EGUchyWw5w9O16A4-AYS9jRoAF77Dg9DIIUxW76Cr4elkMCJNCwdimFAL4kvlwSF0wrLEK-qsVtxQ661MhE8cLwAetdIl8BhfFpxa6hnTjFlhpWTKsQ9os5pX_iPCVlDutDK6kIabkpo0OGtAtxKvtTHJLurAOufNEazzGF1PenkYbBc_bxZ_F5HW2Pmv1a0eT77_6RmyD9HWaDI-y8-y8--f0SsgWCpkeffYHtpc3N37fSAxC3sQt-xfzyzwYQ
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1La9wwEBZpAm0u6TPk0YcOPWQP2sqWZEm9bbc1cduEpUkg9GIkS4YlG2-IN4fNP8q_7EjrXZZCC-3RwowGjeT5xt9oBqH31CS6cpIRqTJHuGWCGC4soQZiZkNdmtlwG_nkNDu-4F8vxeVaqy9QogVJbSTxw6m-cXVXYSD5EMavTcxTm_SlhfAhY4_QlpBJZGgHw7MVgQDIYEEup5wAApDLW3N_kBJ8U9Wu-aY1J5M_RT9X6sXckqv-3cz2q_vfKjf-l_7P0E4HPfFgsVeeow3fvEBPhsuOby_RA3wcIFCOtsLTGv8Y5OfYNA6P3FFR9EgREo0AmzpcgE3nphk7j0fTyTywPt11zo94gMM_OHiaeHwS-1NjAMY4N1UYOZs3ADnbcRsmAJ8X9kiUcRSSzeYTPF6J7uFP4GmvogaAiW_xMDR0CJO1r9BF_uV8eEy6Vg7EMKFmxNfKQ2DohGWpV9RZrbih1luZCp86XoGb1ErXgGd8XXFqqWdMM2aFlZIpx3bRZjNt_B7CVlDutDK6koabmposBG0Au1KvtTHpPurBOpfdUWzLyLKnSRkGl4tfdou_j8jS4OXNorrHX98_-AfZ79Dj0ee8_F6cfjtE24CzVEj2TthrtDm7vfNvAMvM7Nu4a38BbXvy2w
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=Combination+of+RAFT+and+Pd%28II%29-Initiated+Isocyanide+Polymerizations%3A+A+Versatile+Method+for+Facile+Synthesis+of+Helical+Poly%28phenyl+isocyanide%29+Block+and+Star+Copolymers&rft.jtitle=Macromolecules&rft.au=Jiang%2C+Zhi-Qiang&rft.au=Zhao%2C+Song-Qing&rft.au=Su%2C+Yi-Xu&rft.au=Liu%2C+Na&rft.date=2018-02-13&rft.pub=American+Chemical+Society&rft.issn=0024-9297&rft.eissn=1520-5835&rft.volume=51&rft.issue=3&rft.spage=737&rft.epage=745&rft_id=info:doi/10.1021%2Facs.macromol.7b02663&rft.externalDocID=b203896970
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=0024-9297&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=0024-9297&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=0024-9297&client=summon