TY - JOUR
T1 - Diverse self-assembly in soluble oligoazaacenes
T2 - A microscopy study
AU - Richards, Gary J.
AU - Hill, Jonathan P.
AU - Okamoto, Ken
AU - Shundo, Atsuomi
AU - Akada, Misaho
AU - Elsegood, Mark R.J.
AU - Mori, Toshiyuki
AU - Ariga, Katsuhiko
PY - 2009/8/4
Y1 - 2009/8/4
N2 - The synthesis and morphologies of self-assembled aggregates of novel oligoazapentacene 2 and oligoazaheptacene 3 derivatives are reported. Double nucleophilic substitution on 2,3-dicyano-[Hj]-dibenzo-1,4,5,10- te1raazaanthracene 4 gives the corresponding dihydro-oligoacene derivatives, which were then N-alkylated using n-dodecyl bromide to yield self-assembling acene molecules. 2 and 3 self-assemble in solution, leading to a variety of aggregated structures including rolled-up sheets, foams, and fibrous structures reminiscent of organogels. These structures are of substantial interest because of their potential electronic properties and because individual fibers can be "exfoliated". Structures of the aggregates are discussed. Additionally, the crystal structure of precursor 4 is reported because it gives information regarding the intermolecular interactions (hydrogen bonding and intermolecular stacking) in similar compounds. Crystal data for 4: space group P2(1)/n, a = 9.3164(17) Å, b = 7.0649(13) Å, c = 23.684(4) Å, α = 90.00°, β = 99.945(3)°, γ = 90.00°, and V = 1535.4(5)Å3.
AB - The synthesis and morphologies of self-assembled aggregates of novel oligoazapentacene 2 and oligoazaheptacene 3 derivatives are reported. Double nucleophilic substitution on 2,3-dicyano-[Hj]-dibenzo-1,4,5,10- te1raazaanthracene 4 gives the corresponding dihydro-oligoacene derivatives, which were then N-alkylated using n-dodecyl bromide to yield self-assembling acene molecules. 2 and 3 self-assemble in solution, leading to a variety of aggregated structures including rolled-up sheets, foams, and fibrous structures reminiscent of organogels. These structures are of substantial interest because of their potential electronic properties and because individual fibers can be "exfoliated". Structures of the aggregates are discussed. Additionally, the crystal structure of precursor 4 is reported because it gives information regarding the intermolecular interactions (hydrogen bonding and intermolecular stacking) in similar compounds. Crystal data for 4: space group P2(1)/n, a = 9.3164(17) Å, b = 7.0649(13) Å, c = 23.684(4) Å, α = 90.00°, β = 99.945(3)°, γ = 90.00°, and V = 1535.4(5)Å3.
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U2 - 10.1021/la8041633
DO - 10.1021/la8041633
M3 - Article
C2 - 19281267
AN - SCOPUS:68149136941
SN - 0743-7463
VL - 25
SP - 8408
EP - 8413
JO - Langmuir
JF - Langmuir
IS - 15
ER -