Transition-metal-centered monocyclic boron wheel clusters (M©Bn): a new class of aromatic borometallic compounds.

Atomic clusters have intermediate properties between that of individual atoms and bulk solids, which provide fertile ground for the discovery of new molecules and novel chemical bonding. In addition, the study of small clusters can help researchers design better nanosystems with specific physical and chemical properties. From recent experimental and computational studies, we know that small boron clusters possess planar structures stabilized by electron delocalization both in the σ and π frameworks. An interesting boron cluster is B(9)(-), which has a D(8h) molecular wheel structure with a single boron atom in the center of a B(8) ring. This ring in the D(8h)-B(9)(-) cluster is connected by eight classical two-center, two-electron bonds. In contrast, the cluster's central boron atom is bonded to the peripheral ring through three delocalized σ and three delocalized π bonds. This bonding structure gives the molecular wheel double aromaticity and high electronic stability. The unprecedented structure and bonding pattern in B(9)(-) and other planar boron clusters have inspired the designs of similar molecular wheel-type structures. But these mimics instead substitute a heteroatom for the central boron. Through recent experiments in cluster beams, chemists have demonstrated that transition metals can be doped into the center of the planar boron clusters. These new metal-centered monocyclic boron rings have variable ring sizes, M©B(n) and M©B(n)(-) with n = 8-10. Using size-selected anion photoelectron spectroscopy and ab initio calculations, researchers have characterized these novel borometallic molecules. Chemists have proposed a design principle based on σ and π double aromaticity for electronically stable borometallic cluster compounds, featuring a highly coordinated transition metal atom centered inside monocyclic boron rings. The central metal atom is coordinatively unsaturated in the direction perpendicular to the molecular plane. Thus, chemists may design appropriate ligands to synthesize the molecular wheels in the bulk. In this Account, we discuss these recent experimental and theoretical advances of this new class of aromatic borometallic compounds, which contain a highly coordinated central transition metal atom inside a monocyclic boron ring. Through these examples, we show that atomic clusters can facilitate the discovery of new structures, new chemical bonding, and possibly new nanostructures with specific, advantageous properties.

[1]  Lai‐Sheng Wang,et al.  Experimental and computational evidence of octa- and nona-coordinated planar iron-doped boron clusters: Fe©B8− and Fe©B9− , 2012 .

[2]  K. Exner,et al.  Planar hexacoordinate carbon: a viable possibility. , 2000, Science.

[3]  T. Fehlner,et al.  Molecular Clusters: A Bridge to Solid-State Chemistry , 2007 .

[4]  Lai‐Sheng Wang,et al.  Molecular wheel to monocyclic ring transition in boron-carbon mixed clusters C2B6⁻ and C3B5⁻. , 2011, Physical chemistry chemical physics : PCCP.

[5]  J. Oscar C. Jiménez-Halla,et al.  B19-: an aromatic Wankel motor. , 2010, Angewandte Chemie.

[6]  Lai‐Sheng Wang,et al.  Observation of the highest coordination number in planar species: decacoordinated Ta©B10(-) and Nb©B10(-) anions. , 2012, Angewandte Chemie.

[7]  P. Schleyer,et al.  Which NICS aromaticity index for planar pi rings is best? , 2006, Organic letters.

[8]  Alexander I Boldyrev,et al.  A concentric planar doubly π-aromatic B₁₉⁻ cluster. , 2010, Nature chemistry.

[9]  Lai‐Sheng Wang Covalent gold. , 2010, Physical chemistry chemical physics : PCCP.

[10]  A. Boldyrev,et al.  Theoretical design of planar molecules with a nona- and decacoordinate central atom , 2008 .

[11]  Wei Huang,et al.  Carbon avoids hypercoordination in CB6(-), CB6(2-), and C2B5(-) planar carbon-boron clusters. , 2008, Journal of the American Chemical Society.

[12]  Si‐Dian Li,et al.  M@B9 and M@B10 molecular wheels containing planar nona- and deca-coordinate heavy group 11, 12, and 13 metals (M=Ag, Au, Cd, Hg, In, Tl) , 2009 .

[13]  Q. Luo Boron rings containing planar octa- and enneacoordinate cobalt, iron and nickel metal elements , 2008 .

[14]  B. Fokwa,et al.  All-boron planar B6 ring in the solid-state phase Ti7Rh4Ir2B8. , 2012, Angewandte Chemie.

[15]  Lai‐Sheng Wang,et al.  Geometrical requirements for transition-metal-centered aromatic boron wheels: the case of VB10(-). , 2012, Physical chemistry chemical physics : PCCP.

[16]  Truong Ba Tai,et al.  Structure of boron clusters revisited, Bn with n = 14–20 , 2012 .

[17]  Lai‐Sheng Wang,et al.  A photoelectron spectroscopy and ab initio study of B21-: negatively charged boron clusters continue to be planar at 21. , 2012, The Journal of chemical physics.

[18]  J. Chandrasekhar,et al.  Double Aromaticity in the 3,5-Dehydrophenyl Cation and in Cyclo[6]carbon , 1994 .

[19]  Alexander I Boldyrev,et al.  Developing paradigms of chemical bonding: adaptive natural density partitioning. , 2008, Physical chemistry chemical physics : PCCP.

[20]  Thomas Heine,et al.  Unravelling phenomenon of internal rotation in B13+ through chemical bonding analysis. , 2011, Chemical communications.

[21]  Lai‐Sheng Wang,et al.  All-boron analogues of aromatic hydrocarbons: B17- and B18-. , 2011, The Journal of chemical physics.

[22]  T. Heine,et al.  B‐19: An Aromatic Wankel Motor , 2010 .

[23]  Lai‐Sheng Wang,et al.  Experimental and computational evidence of octa- and nona-coordinated planar iron-doped boron clusters: Fe©B8− and Fe©B9− , 2012 .

[24]  Jun Li,et al.  Hydrocarbon analogues of boron clusters — planarity, aromaticity and antiaromaticity , 2003, Nature materials.

[25]  Lai‐Sheng Wang,et al.  Transition-metal-centered nine-membered boron rings: MⓒB9 and MⓒB9(-) (M = Rh, Ir). , 2012, Journal of the American Chemical Society.

[26]  P. Schleyer,et al.  Planar hepta-, octa-, nona-, and decacoordinate first row d-block metals enclosed by boron rings. , 2009, Inorganic chemistry.

[27]  Clémence Corminboeuf,et al.  Nucleus-Independent Chemical Shifts (NICS) as an Aromaticity Criterion , 2006 .

[28]  Alexander I Boldyrev,et al.  Aromatic metal-centered monocyclic boron rings: Co©B8- and Ru©B9-. , 2011, Angewandte Chemie.

[29]  Anastassia N Alexandrova,et al.  Molecular wheel B8(2-) as a new inorganic ligand. photoelectron spectroscopy and ab initio characterization of LiB8(-). , 2004, Inorganic chemistry.

[30]  Lai‐Sheng Wang,et al.  Planarization of B7- and B12- clusters by isoelectronic substitution: AlB6- and AlB11-. , 2011, Journal of the American Chemical Society.

[31]  Anastassia N. Alexandrova,et al.  All-Boron Aromatic Clusters as Potential New Inorganic Ligands and Building Blocks in Chemistry , 2006 .

[32]  J. Chandrasekhar,et al.  Double aromaticity: aromaticity in orthogonal planes. The 3,5-dehydrophenyl cation. , 1979 .

[33]  Zhi‐Xiang Wang,et al.  Construction Principles of "Hyparenes": Families of Molecules with Planar Pentacoordinate Carbons , 2001, Science.

[34]  Lai‐Sheng Wang,et al.  Aluminum avoids the central position in AlB9- and AlB10-: photoelectron spectroscopy and ab initio study. , 2011, The journal of physical chemistry. A.

[35]  Leiming Wang,et al.  CB7−: Experimental and Theoretical Evidence against Hypercoordinate Planar Carbon† , 2007 .

[36]  Lai‐Sheng Wang,et al.  Photoelectron spectroscopy of size‐selected transition metal clusters: Fe−n, n=3–24 , 1995 .

[37]  P. Schleyer,et al.  Cyclic Boron Clusters Enclosing Planar Hypercoordinate Cobalt, Iron, and Nickel , 2009 .

[38]  Lai‐Sheng Wang,et al.  Valence isoelectronic substitution in the B8(-) and B9(-) molecular wheels by an Al dopant atom: umbrella-like structures of AlB7(-) and AlB8(-). , 2011, The Journal of chemical physics.

[39]  Lai‐Sheng Wang,et al.  B22- and B23-: all-boron analogues of anthracene and phenanthrene. , 2012, Journal of the American Chemical Society.

[40]  P. Schleyer,et al.  Boron rings enclosing planar hypercoordinate group 14 elements. , 2007, Journal of the American Chemical Society.

[41]  S. Bulusu,et al.  Planar-to-tubular structural transition in boron clusters: B20 as the embryo of single-walled boron nanotubes. , 2005, Proceedings of the National Academy of Sciences of the United States of America.

[42]  T. Heine,et al.  What is the maximum coordination number in a planar structure? , 2012, Angewandte Chemie.

[43]  Paul von Ragué Schleyer,et al.  Nucleus-Independent Chemical Shifts:  A Simple and Efficient Aromaticity Probe. , 1996, Journal of the American Chemical Society.

[44]  Anastassia N. Alexandrova,et al.  Electronic Structure, Isomerism, and Chemical Bonding in B7 - and B7 , 2004 .

[45]  Lai‐Sheng Wang,et al.  On the analogy of B-BO and B-Au chemical bonding in B11O- and B10Au- clusters. , 2010, The journal of physical chemistry. A.

[46]  G. Frenking,et al.  Aromatic boron wheels with more than one carbon atom in the center: C2B8, C3B9(3+), and C5B11+. , 2005, Angewandte Chemie.

[47]  Leiming Wang,et al.  Experimental and theoretical investigations of CB8-: towards rational design of hypercoordinated planar chemical species. , 2009, Physical chemistry chemical physics : PCCP.