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1
H NMR spectrum of the
product also revealed the formation of a single and symmetrical
product by the appearance of all expected peaks and the neutral
rectangle
of a single and symmetrical product [23].
displayed spectroscopic differences from starting
linkers. Finally, the formation of a [2 + 2] self-assembled product
13
13
was confirmed by MALDI-MS data as evidenced by the peaks
+
at
m
/
z
= 2045.5 and 1957.9 corresponding to [M
+ H
] and [M
-
1
1
PEt
+ MeOH], respectively (M
represents the molar mass of intact
3
1
rectangle).
Density functional theory (DFT) calculation was used to obtain
the energy-minimized view of the neutral rectangle
13
(Fig. 9.8).
Figure 9.8
Energy-optimized structure of
. Ethyl groups have not
been shown for the sake of clarity [23].
13
9.3
3D Molecular Architectures Containing Ethynyl
Functionality: Molecular Prisms
In supramolecular chemistry examples of 3D structures like cages
and prisms are less known unlike the 2D geometries, which are
plenty [1]. A common approach for building a 3D structure is either
a M
combination. Of these two, the former approach is
more common and has been applied in various cases for preparing
3D geometries because of a dearth in tritopic shape-selective Pt/
Pd acceptors [11,20,21,31]. Thus, the design and synthesis of such
tridentate acceptors and their novel 3D structures offer a very
exciting area of research in recent times.
L
or M
L
3
2
2
3
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