메뉴 건너뛰기




Volumn 29, Issue 4, 2009, Pages 185-208

Comments on π-electron conjugation in the five-membered ring of benzo-derivatives of corannulene

Author keywords

Benzo derivatives of corannulene; Corannulene; Cyclic conjugation

Indexed keywords

6-MEMBERED RINGS; BENZO-DERIVATIVE OF CORANNULENE; CORANNULENE; CYCLIC CONJUGATION; ELECTRON CONJUGATION; ENERGY EFFECTS; FIVE-MEMBERED RINGS; STRUCTURAL EFFECT; Π-ELECTRONS;

EID: 70449380763     PISSN: 10406638     EISSN: 15635333     Source Type: Journal    
DOI: 10.1080/10406630903087784     Document Type: Article
Times cited : (16)

References (66)
  • 1
    • 85173703908 scopus 로고
    • Synthese des anti-diperi-Dibenz-coronens und dessen Abbau zum Coronen (Hexabenzo-benzol)
    • Scholl, R. and K. Meyer. 1932. Synthese des anti-diperi-Dibenz-coronens und dessen Abbau zum Coronen (Hexabenzo-benzol). Ber. Dtsch. Chem. Ges. 65:902-915.
    • (1932) Ber. Dtsch. Chem. Ges. , vol.65 , pp. 902-915
    • Scholl, R.1    Meyer, K.2
  • 2
    • 0042488447 scopus 로고
    • Zum Chemismus der Hydridübertragung bei der Schollschen Reaktion
    • Nenitzescu C. D. and A. Balaban. 1958. Zum Chemismus der Hydridübertragung bei der Schollschen Reaktion. Chem. Ber. 91:2109-2116.
    • (1958) Chem. Ber. , vol.91 , pp. 2109-2116
    • Nenitzescu, C.D.1    Balaban, A.2
  • 3
    • 0042504943 scopus 로고
    • Dehydrogenating condensations of aromatics (Scholl and related reactions)
    • ed. G.A. Olah, New York: Wiley-Interscience
    • Balaban, A. T. and C. D. Nenitzescu. 1964. Dehydrogenating condensations of aromatics (Scholl and related reactions), In Friedel-Crafts and related reactions, vol. 2, ed. G.A. Olah, 979-1047. New York: Wiley-Interscience.
    • (1964) Friedel-Crafts and Related Reactions , vol.2 , pp. 979-1047
    • Balaban, A.T.1    Nenitzescu, C.D.2
  • 5
    • 54349109136 scopus 로고    scopus 로고
    • Fluoranthene and its congeners-A graph theoretical study. MATCH Commun
    • Gutman, I. and J. Durdević. 2008. Fluoranthene and its congeners-A graph theoretical study. MATCH Commun. Math. Comput. Chem. 60:659-670.
    • (2008) Math. Comput. Chem. , vol.60 , pp. 659-670
    • Gutman, I.1    Durdević, J.2
  • 6
    • 54949109055 scopus 로고    scopus 로고
    • Hall rule in fluoranthene-type benzenoid hydrocarbons
    • Durdević, J., S. Radenković, and I. Gutman. 2008. Hall rule in fluoranthene-type benzenoid hydrocarbons. J. Serb. Chem. Soc. 73:989-995.
    • (2008) J. Serb. Chem. Soc. , vol.73 , pp. 989-995
    • Durdević, J.1    Radenković, S.2    Gutman, I.3
  • 7
    • 61449115968 scopus 로고    scopus 로고
    • A regularity for cyclic conjugation in acenaphthylene, fluoranthene and their congeners
    • Gutman, I., J. Durdević, and A. T. Balaban. 2009. A regularity for cyclic conjugation in acenaphthylene, fluoranthene and their congeners. Polycycl. Aromat. Comp. 29:3-11.
    • (2009) Polycycl. Aromat. Comp. , vol.29 , pp. 3-11
    • Gutman, I.1    Durdević, J.2    Balaban, A.T.3
  • 9
    • 67650215182 scopus 로고    scopus 로고
    • Verifying the PCP-rule by five-center bond indices
    • Durdević, J., I. Gutman, and R. Ponec. 2009. Verifying the PCP-rule by five-center bond indices. J. Serb. Chem. Soc. 74: 549-554.
    • (2009) J. Serb. Chem. Soc. , vol.74 , pp. 549-554
    • Durdević, J.1    Gutman, I.2    Ponec, R.3
  • 10
    • 68949114966 scopus 로고    scopus 로고
    • Cyclic conjugation in fluoranthene and its benzo-derivatives. Part 1. Catacondensed systems
    • Durdević, J., I. Gutman, J. Terzić, and A. T. Balaban. 2009. Cyclic conjugation in fluoranthene and its benzo-derivatives. Part 1. Catacondensed systems. Polycycl. Aromat. Comp. 29:90-102.
    • (2009) Polycycl. Aromat. Comp. , vol.29 , pp. 90-102
    • Durdević, J.1    Gutman, I.2    Terzić, J.3    Balaban, A.T.4
  • 11
    • 68949121219 scopus 로고    scopus 로고
    • On π-electron conjugation in the five-membered ring of fluoranthene-type benzenoid hydrocarbons
    • submitted
    • Gutman, I. and J. Durdević. 2009. On π-electron conjugation in the five-membered ring of fluoranthene-type benzenoid hydrocarbons. J. Serb. Chem. Soc., submitted.
    • (2009) J. Serb. Chem. Soc.
    • Gutman, I.1    Durdević, J.2
  • 12
    • 67651102988 scopus 로고    scopus 로고
    • Extending the PCP rule. Indian
    • Gutman, I., S. Jeremić, and V. Petrović. 2009. Extending the PCP rule. Indian J. Chem. 48A:658-662.
    • (2009) J. Chem. , vol.48 A , pp. 658-662
    • Gutman, I.1    Jeremić, S.2
  • 13
    • 3242728776 scopus 로고    scopus 로고
    • Partitioning of π-electrons in rings of polycyclic conjugated hydrocarbons. Part 1: Catacondensed benzenoids
    • Randić, M. and A.T. Balaban. 2004. Partitioning of π-electrons in rings of polycyclic conjugated hydrocarbons. Part 1: Catacondensed benzenoids. Polycycl. Aro- mat. Comp. 24:173-193.
    • (2004) Polycycl. Aro- mat. Comp. , vol.24 , pp. 173-193
    • Randić, M.1    Balaban, A.T.2
  • 14
    • 1842679422 scopus 로고    scopus 로고
    • Partitioning of π-electrons in rings of polycyclic benzenoid hydrocarbons. 2. Catacondensed coronoids
    • Balaban, A. T. and M. Randić. 2004. Partitioning of π-electrons in rings of polycyclic benzenoid hydrocarbons. 2. Catacondensed coronoids. J. Chem. Inf. Comp. Sci. 44:50-59.
    • (2004) J. Chem. Inf. Comp. Sci. , vol.44 , pp. 50-59
    • Balaban, A.T.1
  • 15
    • 5444260130 scopus 로고    scopus 로고
    • Partitioning of π-electrons in rings of polycyclic conjugated hydrocarbons.5.Nonalternant hydrocarbons
    • Balaban, A. T. and M. Randić. 2004. Partitioning of π-electrons in rings of polycyclic conjugated hydrocarbons.5.Nonalternant hydrocarbons.J.Chem.Inf.Comp. Sci. 44:1701-1707.
    • (2004) J.Chem.Inf.Comp. Sci. , vol.44 , pp. 1701-1707
    • Balaban, A.T.1
  • 16
    • 4243160739 scopus 로고    scopus 로고
    • Partitioning of π-electrons in rings of poly- cyclic conjugated hydrocarbons. Part 3. Perifusenes
    • Balaban, A. T. and M. Randić. 2004. Partitioning of π-electrons in rings of poly- cyclic conjugated hydrocarbons. Part 3. Perifusenes. New J. Chem. 28:800-806.
    • (2004) New J. Chem. , vol.28 , pp. 800-806
    • Balaban, A.T.1
  • 17
    • 17744400498 scopus 로고    scopus 로고
    • Partitioning of π-electrons in rings of poly- cyclic conjugated hydrocarbons. 6. Comparisons with other methods for estimating the local aromaticity of rings in polycyclic benzenoids
    • Balaban, A. T. and M. Randić. 2005. Partitioning of π-electrons in rings of poly- cyclic conjugated hydrocarbons. 6. Comparisons with other methods for estimating the local aromaticity of rings in polycyclic benzenoids. J. Math. Chem. 32:443- 453.
    • (2005) J. Math. Chem. , vol.32 , pp. 443-453
    • Balaban, A.T.1
  • 19
    • 0021201255 scopus 로고
    • Molecular structure of 5,10-dimethoxybenzo[j]fluoranthene
    • Briant, C. E., R. L. Edwards, D. W. Jones, and W. S. McDonald. 1984. Molecular structure of 5,10-dimethoxybenzo[j]fluoranthene. Carcinogenesis 5:1041-1045.
    • (1984) Carcinogenesis , vol.5 , pp. 1041-1045
    • Briant, C.E.1    Edwards, R.L.2    Jones, D.W.3    Mcdonald, W.S.4
  • 20
    • 11144297745 scopus 로고    scopus 로고
    • Cyclic conjugation in benzo-annelated perylenes: How empty is the "empty" ring?
    • Gutman, I., N. Turković, and J. Jovilić. 2004. Cyclic conjugation in benzo-annelated perylenes: How empty is the "empty" ring? Monatshefte für Chemie 135:1389-1394.
    • (2004) Monatshefte für Chemie , vol.135 , pp. 1389-1394
    • Gutman, I.1    Turković, N.2
  • 21
    • 0000219566 scopus 로고
    • π-Electron"ringcurrents"influorantheneandrelatedmolecules
    • Mallion, R.B.1970.π-Electron"ringcurrents"influorantheneandrelatedmolecules. J. Mol. Spectr. 35: 491-493.
    • (1970) J. Mol. Spectr. , vol.35 , pp. 491-493
    • Mallion, R.B.1
  • 22
    • 0035933339 scopus 로고    scopus 로고
    • Theoretical stud- ies on the effectg of sequential benzannuletion to corannulene
    • Dinadayalane, T. C., U. D. Priyakimar, and G. N. Sastry. 2001. Theoretical stud- ies on the effectg of sequential benzannuletion to corannulene. J. Mol. Struct. Theochem. 543:1-10.
    • (2001) J. Mol. Struct. Theochem. , vol.543 , pp. 1-10
    • Dinadayalane, T.C.1    Priyakimar, U.D.2    Sastry, G.N.3
  • 23
    • 0037189246 scopus 로고    scopus 로고
    • Structure−energy relationships in curved polycyclic aromatic hydrocarbons: Study of benzocorannulenes
    • Dinadayalane, T. C. and G. N. Sastry. 2002. Structure−energy relationships in curved polycyclic aromatic hydrocarbons: Study of benzocorannulenes. J. Org. Chem. 67:4605-4607.
    • (2002) J. Org. Chem. , vol.67 , pp. 4605-4607
    • Dinadayalane, T.C.1    Sastry, G.N.2
  • 24
    • 33748928804 scopus 로고    scopus 로고
    • Computational studies on siblings en-route to fullerenes: Study of curved polycyclic aromatic hydrocarbons
    • Sastry, G. N. 2006. Computational studies on siblings en-route to fullerenes: Study of curved polycyclic aromatic hydrocarbons. J. Mol. Struc. Theochem. 771:141-147.
    • (2006) J. Mol. Struc. Theochem. , vol.771 , pp. 141-147
    • Sastry, G.N.1
  • 25
    • 0001556420 scopus 로고
    • Heterocirculenes a new class of polycyclic aromatic hydrocarbons
    • Dopper, J. H. and H. Wynberg. 1972. Heterocirculenes a new class of polycyclic aromatic hydrocarbons. Tetrahedron Lett. 13:763-766.
    • (1972) Tetrahedron Lett. , vol.13 , pp. 763-766
    • Dopper, J.H.1    Wynberg, H.2
  • 26
    • 0012857956 scopus 로고
    • Synthesis and properties of some heterocirculenes
    • Dopper, J. H. and H. Wynberg. 1975. Synthesis and properties of some heterocirculenes. J. Org. Chem. 40:1957-1966.
    • (1975) J. Org. Chem. , vol.40 , pp. 1957-1966
    • Dopper, J.H.1    Wynberg, H.2
  • 27
    • 0001354707 scopus 로고
    • Use of thieno[2,3-b]thiophene in the synthesis of heterohelicenes by double photocyclizations
    • Dopper, J. H., D. Oudman, and H. Wynberg. 1973. Use of thieno[2,3-b]thiophene in the synthesis of heterohelicenes by double photocyclizations. J. Am. Chem. Soc. 95:3692-3698.
    • (1973) J. Am. Chem. Soc. , vol.95 , pp. 3692-3698
    • Dopper, J.H.1    Oudman, D.2    Wynberg, H.3
  • 29
    • 33846230048 scopus 로고    scopus 로고
    • Geodesic polyarenes by flash vacuum pyrolysis
    • Tsefrikas, V. M. and L. T. Scott. 2006. Geodesic polyarenes by flash vacuum pyrolysis. Chem. Rev. 106:4866-4884.
    • (2006) Chem. Rev. , vol.106 , pp. 4866-4884
    • Tsefrikas, V.M.1    Scott, L.T.2
  • 30
    • 0000127624 scopus 로고    scopus 로고
    • Buckybowls: Polynuclear aromatic hydrocar- bons related to the buckminsterfullerene surface
    • Rabideau, P. W. and A. Sygula. 1996. Buckybowls: Polynuclear aromatic hydrocar- bons related to the buckminsterfullerene surface. Accounts Chem. Res. 29:235-242.
    • (1996) Accounts Chem. Res. , vol.29 , pp. 235-242
    • Rabideau, P.W.1    Sygula, A.2
  • 31
    • 0001839540 scopus 로고    scopus 로고
    • Quest for'bucky-balls' and'bucky-bowls': An odyssey through the science of organic synthesis
    • Mehta, G. and G. Panda. 1998. Quest for'bucky-balls' and'bucky-bowls': an odyssey through the science of organic synthesis. Proc. Indian Natl. Sci. Acad. A, Phys. Sci. 64:587-608.
    • (1998) Proc. Indian Natl. Sci. Acad. A, Phys. Sci. , vol.64 , pp. 587-608
    • Mehta, G.1    Panda, G.2
  • 35
    • 84948376420 scopus 로고
    • Extended systems of closed helicene. Synthesis and characterization of [7] and [7.7]-circulene
    • Yamamoto K. 1993. Extended systems of closed helicene. Synthesis and characterization of [7] and [7.7]-circulene. Pure Appl. Chem. 65:157-173.
    • (1993) Pure Appl. Chem. , vol.65 , pp. 157-173
    • Yamamoto, K.1
  • 36
    • 33947335857 scopus 로고
    • Dibenzo[ghi,mno]fluoranthene
    • Barth, W. E. and R. G. Lawton. 1966. Dibenzo[ghi,mno]fluoranthene. J. Am. Chem.Soc. 88:380-381.
    • (1966) J. Am. Chem.Soc. , vol.88 , pp. 380-381
    • Barth, W.E.1    Lawton, R.G.2
  • 37
    • 33947292488 scopus 로고
    • Synthesis of corannulene
    • Lawton, R. G. and W. E. Barth. 1971. Synthesis of corannulene. J. Am. Chem. Soc. 93:1730-1745.
    • (1971) J. Am. Chem. Soc. , vol.93 , pp. 1730-1745
    • Lawton, R.G.1    Barth, W.E.2
  • 38
    • 0028803144 scopus 로고
    • Formation of [60]fullerene by pyrolysis of corannulene, 7,10-bis(2,2'-dibromovinyl)fluoranthene, and 11,12-benzofluoranthene
    • Crowley, C., H. W. Kroto, R. Taylor, D. R. M. Walton, M. S. Bratcher, P. Cheng, and L. T. Scott. 1995. Formation of [60]fullerene by pyrolysis of corannulene, 7,10-bis(2,2'-dibromovinyl)fluoranthene, and 11,12-benzofluoranthene. Tetrahedron Lett. 36:9215-9218.
    • (1995) Tetrahedron Lett. , vol.36 , pp. 9215-9218
    • Crowley, C.1    Kroto, H.W.2    Taylor, R.3    Walton, D.R.M.4    Bratcher, M.S.5    Cheng, P.6    Scott, L.T.7
  • 40
    • 0031585060 scopus 로고    scopus 로고
    • A new synthesis of corannulene
    • Mehta, G., and G. Panda. 1997. A new synthesis of corannulene. Tetrahedron Lett 38:2145-2148.
    • (1997) Tetrahedron Lett. , vol.38 , pp. 2145-2148
    • Mehta, G.1    Panda, G.2
  • 41
    • 0029978631 scopus 로고    scopus 로고
    • Corannulene synthesis via the pyrolysis of silyl vinyl ethers
    • Liu, C. Z. and P. W. Rabideau. 1996. Corannulene synthesis via the pyrolysis of silyl vinyl ethers. Tetrahedron Lett. 37:3437-3440.
    • (1996) Tetrahedron Lett. , vol.37 , pp. 3437-3440
    • Liu, C.Z.1    Rabideau, P.W.2
  • 44
    • 0028302424 scopus 로고
    • Synthesis and hydropyrolysisofbis-trimethylsilylsubstituted3-(4Hcyclopenta[def]phenanthryli- dene)-1,4-pentadiyne. A new route to corannulene
    • Zimmermann, G., U. Nuechter, S. Hagen, and M. Nuechter. 1994. Synthesis and hydropyrolysisofbis-trimethylsilylsubstituted3-(4Hcyclopenta[def]phenanthryli- dene)-1,4-pentadiyne. A new route to corannulene. Tetrahedron Lett. 35:4747-4750.
    • (1994) Tetrahedron Lett. , vol.35 , pp. 4747-4750
    • Zimmermann, G.1    Nuechter, U.2    Hagen, S.3    Nuechter, M.4
  • 47
    • 0034614344 scopus 로고    scopus 로고
    • Bucky-bowls. A general approach to benzo-corannulenes: Synthesis of mono-, di- and tri-benzocorannulenes
    • Mehta, G. and P. V. V. S. Sarma. 2000. Bucky-bowls. A general approach to benzo-corannulenes: synthesis of mono-, di- and tri-benzocorannulenes. Chem. Commun. 19-20.
    • (2000) Chem. Commun. , pp. 19-20
    • Mehta, G.1    Sarma, P.V.V.S.2
  • 50
    • 0000242437 scopus 로고
    • Buckybowls: Synthesis and ab initio calculated structure of the first semibuckminsterfullerene
    • Rabideau, P. W., A. H. Abdourazak, H. E. Folsom, Z. Marcinow, A. Sygula, and R. Sygula. 1994. Buckybowls: Synthesis and ab initio calculated structure of the first semibuckminsterfullerene. J. Am. Chem. Soc. 116:7891-7892.
    • (1994) J. Am. Chem. Soc. , vol.116 , pp. 7891-7892
    • Rabideau, P.W.1    Abdourazak, A.H.2    Folsom, H.E.3    Marcinow, Z.4    Sygula, A.5    Sygula, R.6
  • 51
    • 32944460933 scopus 로고    scopus 로고
    • Computational studies on the cyclization of polycyclic aromatic hydrocarbons in the synthesis of curved aromatic derivatives
    • Bunuel, E., J. Marco-Martinez, S. Diaz-Tendero, F. Martin, M. Acalmi, and D. J. Cardenas. 2006. Computational studies on the cyclization of polycyclic aromatic hydrocarbons in the synthesis of curved aromatic derivatives. ChemPhysChem 7:475-481.
    • (2006) ChemPhysChem , vol.7 , pp. 475-481
    • Bunuel, E.1    Marco-Martinez, J.2    Diaz-Tendero, S.3    Martin, F.4    Acalmi, M.5    Cardenas, D.J.6
  • 52
    • 85021622022 scopus 로고
    • Corannulene bowl-to-bowl inversion is rapid at room temperature
    • Scott, L. T., M. M. Hashemi, and M. S. Bratcher. 1992. Corannulene bowl-to-bowl inversion is rapid at room temperature. J. Am. Chem. Soc. 114:1920-1921.
    • (1992) J. Am. Chem. Soc. , vol.114 , pp. 1920-1921
    • Scott, L.T.1    Hashemi, M.M.2    Bratcher, M.S.3
  • 54
    • 0035955409 scopus 로고    scopus 로고
    • Groundwork for a rational synthesis of C60: Cyclodehydrogenation of a C60H30 polyarene
    • Boorum, M. M., Y. V. Vasiliev, T. Drewello, and L. T. Scott. 2001. Groundwork for a rational synthesis of C60: cyclodehydrogenation of a C60H30 polyarene. Science 294:828-831.
    • (2001) Science , vol.294 , pp. 828-831
    • Boorum, M.M.1    Vasiliev, Y.V.2    Drewello, T.3    Scott, L.T.4
  • 55
    • 0000061225 scopus 로고    scopus 로고
    • Semiempirical SCF MO study of bowl-to-bowl inversion in corannulene and smaller circulenes
    • Yavari, I., E. Taj-Khorshid, D. Nori-DShargh, and S. Balalaie. 1997. Semiempirical SCF MO study of bowl-to-bowl inversion in corannulene and smaller circulenes. J. Mol. Struct. Theochem 393:163-166.
    • (1997) J. Mol. Struct. Theochem. , vol.393 , pp. 163-166
    • Yavari, I.1    Taj-Khorshid, E.2    Nori-Dshargh, D.3    Balalaie, S.4
  • 56
    • 25144432424 scopus 로고    scopus 로고
    • Coordination chemistry of buckybowls: From corannulene to a hemifullerene
    • Petrukhina, M. A. and L. T. Scott. 2005. Coordination chemistry of buckybowls: from corannulene to a hemifullerene. Dalton Trans. 2969-2975.
    • (2005) Dalton Trans. , pp. 2969-2975
    • Petrukhina, M.A.1    Scott, L.T.2
  • 57
    • 3242739060 scopus 로고    scopus 로고
    • Creation of hoop- and bowl-shaped benzenoid systems by selective detraction of [60]fullerene conjugation. [10]cyclophenacene and fused corannulene derivatives
    • Matsuo, Y., K. Tahara, M. Sawamura, and E. Nakamura. 2004. Creation of hoop- and bowl-shaped benzenoid systems by selective detraction of [60]fullerene conjugation. [10]cyclophenacene and fused corannulene derivatives. J. Am. Chem. Soc. 126:8725-8734.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 8725-8734
    • Matsuo, Y.1    Tahara, K.2    Sawamura, M.3    Nakamura, E.4
  • 59
    • 0029271689 scopus 로고
    • Thermochemical properties of curved PAH and fullerenes: A group additivity method compared with MM3(92) and MOPAC predictions
    • Pope, C. J. and J. B. Howard. 1995. Thermochemical properties of curved PAH and fullerenes: A group additivity method compared with MM3(92) and MOPAC predictions. J. Phys. Chem. 99:4306-4316.
    • (1995) J. Phys. Chem. , vol.99 , pp. 4306-4316
    • Pope, C.J.1    Howard, J.B.2
  • 60
    • 4644317796 scopus 로고    scopus 로고
    • Accurate and efficient method for predicting thermochemistry of polycyclic aromatic hydrocarbons-bond-centered group additivity
    • Yu, J., R. Sumathi, and W. H. Green. 2004. Accurate and efficient method for predicting thermochemistry of polycyclic aromatic hydrocarbons-bond-centered group additivity. J. Am. Chem. Soc. 126:12685-12700.
    • (2004) J. Am. Chem. Soc. , vol.126 , pp. 12685-12700
    • Yu, J.1    Sumathi, R.2    Green, W.H.3
  • 61
    • 21144453462 scopus 로고    scopus 로고
    • Cyclic conjugation energy effects in polycyclic π-electron systems
    • Gutman, I. 2005. Cyclic conjugation energy effects in polycyclic π-electron systems. Monatsh. Chem. 135:1055-1069.
    • (2005) Monatsh. Chem. , vol.135 , pp. 1055-1069
    • Gutman, I.1
  • 64
    • 34250806067 scopus 로고    scopus 로고
    • Mathematics of periodic tables of benzenoid hydrocarbons
    • Dias, J. R. 2007. Mathematics of periodic tables of benzenoid hydrocarbons. J. Chem. Inf. Comput. Model. 47:707-715.
    • (2007) J. Chem. Inf. Comput. Model , vol.47 , pp. 707-715
    • Dias, J.R.1
  • 65
    • 0141789719 scopus 로고    scopus 로고
    • Aromaticity of polycyclic conjugated hydrocarbons
    • Randić, M. 2003. Aromaticity of polycyclic conjugated hydrocarbons. Chem. Rev. 103:3449-3606.
    • (2003) Chem. Rev. , vol.103 , pp. 3449-3606
    • Randić, M.1
  • 66
    • 33846206028 scopus 로고    scopus 로고
    • Aromatic molecular-bowl hydrocarbons: Synthetic derivatives, their structures, and physical properties
    • Wu, M., and J. S. Siegel. 2006. Aromatic molecular-bowl hydrocarbons: synthetic derivatives, their structures, and physical properties. Chem. Rev. 106:4843-4867
    • (2006) Chem. Rev. , vol.106 , pp. 4843-4867
    • Wu, M.1    Siegel, J.S.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.