参考文献

［1］G. R. Desiraju，T. Steiner，The weak hydrogen bond in structural chemistry and biology. Oxford University Press，Oxford，1999.

［2］G.A.Jeffrey，An introduction to hydrogen bonding.Oxford University Press，New York，1997.

［3］T. Steiner，G. R. Desiraju，Distinction between the weak hydrogen bond and the van der Waals interaction.Chem.Commun.1998，891-892.

［4］G. R. Desiraju，C—H…O and other weak hydrogen bonds. From crystal engineering to virtual screening.Chem.Commun.2005，2995-3001.

［5］D.-Y. Wang，J.-L. Wang，D.-W. Zhang，Z.-T. Li，N—H…X （X=F，Cl，Br，and I） Hydrogen bonding in aromatic amide derivatives in crystal structures.Sci.China Chem.2012，55，2018-2026.

［6］P. Du，X.-K. Jiang，Z.-T. Li，Five- and six-membered N-H…S hydrogen bonding in aromatic amides.Tetrahedron Lett.2009，50，320-324.

［7］D.-W. Zhang，X. Zhao，J.-L. Hou，Z.-T. Li，Aromatic amide foldamers： structures，properties，and functions.Chem.Rev.2012，112，5271-5316.

［8］P. Ottiger，C. Pfaffen，R. Leist，S. Leutwyler，R. A. Bachorz，W. Klopper，Strong N—H…π hydrogen bonding in amide-benzene interactions.J.Phys.Chem.B2009，113，2937-2943.

［9］A. L. Ringer，M. S. Figgs，M. O. Sinnokrot，C. Sherrill，Aliphatic C-H/π interactions： methane-benzene，methane-phenol，and methane-indole complexes.J.Phys.Chem.A2006，110，10822-10828.

［10］J. Cheng，C. Kang，W. Zhu，X. Luo，C. M. Puah，K. Chen，J. Shen，H. Jiang，N-methylformamide-benzene complex as a prototypical peptide N-H…π hydrogen-bonded system： density functional theory and MP₂studies.J.Org.Chem.2003，68，7490-7495.

［11］S. A. Fairhurst，R. A. Henderson，D. L. Hughes，S. K. Ibrahim，C. J. Pickett，An intramolecularhydrogen bond？ Electrosynthesis and X-ray crystallographic structure of ［WH₃（η¹-OCOMe）（Ph₂PCH₂CH₂PPh₂）₂］.J.Chem.Soc.Chem.Commun.1995，1569-1570.

［12］L. Brammer，J. M. Charnock，P. L. Goggin，R. J. Goodfellow，A. G. Orpen，T. F. Koetzle，The role of transition metal atoms as hydrogen bond acceptors： a neutron diffraction study of［PtCl₄］·cis-［PtCl₂（NH₂Me）₂］at 20 K.J.Chem.Soc.Dalton Trans.1991，1789-1798.

［13］J.D.Dunitz，Organic fluorine：odd man out.ChemBioChem2004，5，614-621.

［14］C. Li，S.-F. Ren，J.-L. Hou，H.-P. Yi，S.-Z. Zhu，X.-K. Jiang，Z.-T. Li，F…H-N Hydrogen bonding driven foldamers：efficient receptors for dialkylammonium ions.Angew.Chem.Int.Ed.2005，44，5725-5729.

［15］B.-Y. Lu，Y.-Y. Zhu，Z.-M. Li，X. Zhao，Z.-T. Li，Assessment of the intramolecular C-H…X （X=F，Cl，Br） hydrogen bonding of 1，4-diphenyl-1，2，3-triazoles.Tetrahedron2012，68，8857-8862.

［16］Y.-H. Liu，L. Zhang，X.-N. Xu，Z.-M. Li，D.-W. Zhang，X. Zhao，Z.-T. Li，Intramolecular C-H…F hydrogen bonding-induced 1，2，3-triazole-based foldamers.Org.Chem.Front.2014，1，494-500.

［17］M. C. Etter，Encoding and decoding hydrogen-bond patterns of organic compounds.Acc. Chem. Res.1990，23，120-126.

［18］M.C.Etter，Hydrogen bonds as design elements in organic chemistry.J.Phys.Chem.1991，95，4601-4610.

［19］S. V. Kolotuchin，P. A. Thiessen，E. E. Fenlon，S. R. Wilson，C. J. Loweth，S. C. Zimmerman，Self-assembly of 1，3，5-benzenetricarboxylic（trimesic）acid and its analogues.Chem.Eur.J.1999，5，2537-2547.

［20］B. Omondi，M. A. Fernandes，M. Layh，D. C. Levendis，Cocrystal ofcis- andtrans-N-phenyl formamide.Acta Cryst.C2008，64，o137-o138.

［21］L. S. Reddy，S. Basavoju，V. R. Vangala，A. Nangia，Hydrogen bonding in crystal structures ofN，N'-bis（3-pyridyl）urea. Why is the N—H…O tape synthon absent in diaryl ureas with electron-withdrawing groups？Cryst.Growth Des.2006，6，161-173.

［22］S. Garg，J. M. Shreeve，Trifluoromethyl- or pentafluorosulfanyl-substituted poly -1，2，3-triazole compounds as dense stable energetic materials.J.Mater.Chem.2011，21，4787-4795.

［23］M. S. Costa，N. Boechat，V. F. Ferreira，S. M. S. V. Wardell，J. M. S. Skakle，4-Difluoro-methyl-1-（4-methyl-phenyl）-1H-1，2，3-triazole.Acta Crystallogr.E2006，62，o1925-o1927.

［24］D.-Y. Wang，L.-Y. You，J.-L. Wang，H. Wang，D.-W. Zhang，Z.-T. Li，Complexation of two macrocycles for amide，saccharide，and halide derivatives： The capacity of 1，2，3-triazole as hydrogen and halogen bonding acceptors.Tetrahedron Lett.2013，54，6967-6970.

［25］S. H. Gellman，G. P. Dado，C.-B. Liang，B. R. Adam，Conformation-directing effects of a single intramolecular amide-amide hydrogen bond： variable-temperature NMR and IR studies on a homologous diamide series.J.Am.Chem.Soc.1991，113，1164-1173.

［26］齐志齐，绍学斌，赵新，李晓强，王晓钟，张未星，蒋锡夔，黎占亭，四氢键二聚体和分子识别.有机化学2003，23，403-412.

［27］Y. Hamuro，S. J. Geib，A. D. Hamilton，Oligoanthranilamides. non-peptide subunits that show formation of specific secondary structure.J.Am.Chem.Soc.1996，118，7529-7541.

［28］Y.-Y. Zhu，H.-P. Yi，C. Li，X.-K. Jiang，Z.-T. Li，The N—H…X （X=Cl，Br and I） hydrogen bonding in aromatic amides：a crystallographic and¹H NMR study.Cryst.Growth Des.2008，8，1294-1300.

［29］Y.-Y. Zhu，L. Jiang，Z.-T. Li，Intramolecular six-membered N—H…Br and N—H…I hydrogen bonding in aromatic amides.CrystEngComm2009，11，235-238.

［30］G. N. Tew，R. W. Scott，M. L. Klein，W. F. DeGrado，De novo design of antimicrobial polymers，foldamers，and small molecules：from discovery to practical applications.Acc.Chem.Res.210，43，30-39.

［31］D. Zornik，R. M. Meudtner，T. El Malah，C. M. Thiele，S. Hecht，Designing structural motifs for clickamers：exploiting the 1，2，3-triazole moiety to generate conforma- tionally restricted molecular architecturesChem. Eur.J.2011，17，1473-1484.

［32］S. C. Zimmerman，P. S. Corbin，Heteroaromatic modules for self-assembly using multiple hydrogen bonds.Struct.&Bond.2000，96，63-94.

［33］S.-K. Chang，D. V. Engen，E. Fan，A. D. Hamilton，Hydrogen bonding and molecular recognition： Synthetic，complexation，and structural studies on barbiturate binding to an artificial receptor.J.Am.Chem.Soc.1991，113，7640-7645.

［34］C. Roberts，R. Bandaru，C. Switzer，Theoretical and experimental study of isoguanine and isocytosine： base pairing in an expanded genetic system.J.Am.Chem.Soc.1997，119，4640-4649.

［35］T. J. Murray，S. C. Zimmerman，S. V. Kolotuchin，Synthesis of heterocyclic compounds containing three contiguous hydrogen bonding sites in all possible arrangements.Tetrahedron1995，51，635-648.

［36］B. A. Blight，A. Camara-Campos，S. Djurdjevic，M. Kaller，D. A. Leigh，F. M. McMillan，H. McNab，A. M. Slawin，AAA-DDD triple hydrogen bond complexes.J.Am.Chem.Soc.2009，131，14116-14122.

［37］F. H. Beijer，H. Kooijman，A. L. Spek，R. P. Sijbesma，E. W. Meijer，Self- complementarity achieved through quadruple hydrogen bonding.Angew.Chem.Int.Ed.1998，37，75-78.

［38］Y. Yang，H. J. Yan，C.-F. Chen，L.-J. Wan，Quadruply hydrogen-bonded building block from hydrazide-quinolinone motif and gelation ability of its analogous oxalic monoester-monoamide derivative.Org. Lett.2007，9，4991-4994.

［39］R.P.Sijbesma，E.W.Meijer，Quadruple hydrogen bonded systems.Chem.Commun.2003，5-16.

［40］S. H. M. S?ntjens，R. P. Sijbesma，M. H. P. van Genderen，E. W. Meijer，Stability and lifetime of quadruply hydrogen bonded 2-ureido-4［1H］-pyrimidinone dimmers.J.Am.Chem.Soc.2000，122，7487-7493.

［41］P. S. Corbin，L. J. Lawless，Z. Li，Y. Ma，M. J. Witmer，S. C. Zimmerman，Discrete and polymeric self-assembled dendrimers： Hydrogen bond-mediated assembly with high stability and high fidelityProc. Natl.Acad.Sci.USA2002，99，5099-5104.

［42］P. S. Corbin，S. C. Zimmerman，P. A. Thiessen，N. A. Hawryluk，T. J. Murray，Complexation-induced unfolding of heterocyclic ureas. Simple foldamers equilibrate with multiply hydrogen-bonded sheetlike structuresJ.Am.Chem.Soc.2001，123，10475-10488.

［43］U.Lüning，C.Kühl，Heterodimers for molecular recognition by fourfold hydrogen bonds.Tetrahedron Lett.1998，39，5735-5738.

［44］X. Zhao，X.-Z. Wang，X.-K. Jiang，Y.-Q. Chen，Z.-T. Li，G.-J. Chen，Hydrazide -based quadruply hydrogen-bonded heterodimers. Structure，assembling selectivity，and supramolecular substitution.J. Am. Chem.Soc.2003，125，15128-15139.

［45］Y. Yang，Z.-Y. Yang，Y.-P. Yi，J.-F. Xiang，C.-F. Chen，L.-J. Wan，Z.-G. Shuai，Helical molecular duplex strands： multiple hydrogen-bond-mediated assembly of self -complementary oligomeric hydrazide derivatives.J.Org.Chem.2007，72，4936-4946.

［46］Y. Hisamatsu，N. Shirai，S.-i. Ikeda，K. Odashima，A new quadruple hydrogen- bonding module based on five-membered heterocyclic urea structure.Org.Lett.2010，12，1776-1779.

［47］J. Taubitz，U. Lüning，On the importance of the nature of hydrogen bond donors in multiple hydrogen bond systems.Eur.J.Org.Chem.2008，5922-5927.

［48］J. Taubitz，U. Lüning，The AAAA·DDDD hydrogen bond dimer. Synthesis of a soluble sulfurane as AAAA domain and generation of a DDDD counterpart，Aust.J.Chem.2009，62，1550-1555.

［49］B. A. Blight，C. A. Hunter，D. A. Leigh，H. McNab，P. I. T. Thomson，An AAAA- DDDD quadruple hydrogen-bond array.Nat.Chem.2011，3，244-248.

［50］D. A. Leigh，C. C. Robertson，A. M. Z. Slawin，P. I. T. Thomson，AAAA-DDDD quadruple hydrogen-bond arrays featuring NH…N and CH…N hydrogen bonds.J.Am.Chem.Soc.2013，135，9939-9943.

［51］J.S.Nowick，Chemical models of protein β-Sheets.Acc.Chem.Res.1999，32，287-296.

［52］T. Moriuchi，T. Tamura，T. Hirao，Self-assembly of dipeptidyl ureas： A new class of hydrogen-bonded molecular duplexes.J.Am.Chem.Soc.2002，124，9356-9357.

［53］Y. Yang，W.-J. Chu，J.-W. Liu，C.-F. Chen，Hydrazide as an excellent hydrogen bonding building block in supramolecular chemistry.Curr.Org.Chem.2011，15，1302-1313.

［54］B.Gong，Molecular duplexes with encoded sequences and stabilities.Acc.Chem.Res.2012，45，2077-2087.

［55］B. Gong，Y. Yan，H. Zeng，E. Skrzypczak-Jankunn，Y. W. Kim，J. Zhu，H. Ickes，A new approach for the design of supramolecular recognition units：Hydrogen-bonded molecular duplexes.J.Am.Chem.Soc.1999，121，5607-5608.

［56］P. Zhang，H. Chu，X. Li，W. Feng，P. Deng，L. Yuan，B. Gong，Alternative strategy for adjusting the association specificity of hydrogen-bonded duplexes.Org.Lett.2011，13，54-57.

［57］H. Zeng，H. Ickes，R. A. Flowers，Ⅱ，B. Gong，Sequence specificity of hydrogen-bonded molecular duplexes.J.Org.Chem.2001，66，3574-3583.

［58］Y. Yang，J.-F. Xiang，M. Xue，H.-Y. Hu，C.-F. Chen，Supramolecular substitution reactions between hydrazide-based molecular duplex strands： Complexation induced nonsymmetry and dynamic behavior.J. Org.Chem.2007，72，6369-6377.

［59］Y. Yang，T. Chen，J.-F. Xiang，H.-J. Yan，C.-F. Chen，L.-J. Wan，Mutual responsive hydrazide- based low-molecular-mass organic gelators：Probing gelation on the molecular level.Chem.Eur.J.2008，14，5742-5746.

［60］A. P. Bisson，F. J. Carver，D. S. Eggleston，R. C. Haltiwanger，C. A. Hunter，D. L. Livingstone，J. F. McCabe，C. Rotger，A. E. Rowan，Synthesis and recognition properties of aromatic amide oligomers： Molecular zippers.J.Am.Chem.Soc.2000，122，8856-8868.

［61］Y.-X. Xu，T.-G. Zhan，X. Zhao，Z.-T. Li，Hydrogen bonding-driven highly stable homoduplexes formed by benzene/naphthalene amide oligomers.Org.Chem.Front.2014，1，73-78.

［62］E.R.B.Kabir，E.N.Ferdous，Kevlar-The super tough fiber，Int.J.Text.Sci.2012，1，78-83.

［63］Z.-M. Shi，S.-G. Chen，X. Zhao，X.-K. Jiang，Z.-T. Li，Meta-substituted benzamide oligomers that complex mono-，di-and tricarboxylates：folding-induced selectivity and chirality.Org.Biomol.Chem.2011，9，8122-8129.

［64］J. Zhu，J.-B. Lin，Y.-X. Xu，X.-B. Shao，X.-K. Jiang，Z.-T. Li，Hydrogen-bonding- mediated anthranilamide homoduplexes. Increasing stability through preorganization and iterative arrangement of simple amide binding sites.J.Am.Chem.Soc.2006，128，12307-12313.

［65］E. A. Archer，M. J. Krische，Duplex oligomers defined via covalent casting of a one-dimensional hydrogen-bonding motif.J.Am.Chem.Soc.2002，124，5074-5083.

［66］H. Gong，M. J. Krische，Duplex molecular strands based on the 3，6-diamino- pyridazine hydrogen bonding motif： Amplifying small-molecule self-assembly preferences through preorganization and iterative arrangement of binding residues.J.Am.Chem.Soc.2005，127，1719-1725.

［67］J. Sartorius，H.-J. Schneider，A general scheme based on empirical increments for the prediction of hydrogen-bond associations of nucleobases and of synthetic host-guest complexes.Chem.Eur.J.1996，2，1446-1462.