Magnetic Properties of Metallomesogens: In 2 parts. Part II. Phase Behaviours and Luminescent Properties

292 Pages·33.053 MB·Russian

by  Galyametdinov Y.

Copyright ООО «ЦКБ «БИБКОМ» & ООО «Aгентство Kнига-Cервис»
Ministry of Science and Higher Education of the Russian Federation
«Kazan National Research Technological Univesity»

Y. Galyametdinov, N. Selivanova, A. Knyazev

M A G N E T I C P R O P E R T I E S
O F M E T A L L O M E S O G E N S

Part II

PHASE BEHAVIOURS
AND LUMINESCENT PROPERTIES

Kazan
KNRTU Press

2020
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UDC 546.443.03
LBC G 122-26

It is published by decision of the Editorial and Publishing Council of Kazan National
Research Technological University

Reviewers:
PhD in Chemical Sciences, Professor, I. S. Antipin
PhD in Chemical Sciences, Professor, L. Y. Zakharova

Galyametdinov Y.
Magnetic Properties of Metallomesogens : monograph : in 2 p.
Part II. Phase Behaviours and Luminescent Properties / Y. Gal-
yametdinov, N. Selivanova, A. Knyazev; Ministry of Education
and Science of Russia, Kazan National Research Technological
University. – Kazan : KNRTU Press, 2020. – 292 p.

ISBN 978-5-7882-2796-2
ISBN 978-5-7882-2798-6 (ч. II)

The monograph presents the published works results on the creation and study of
metal-containing liquid crystals – metallomesogens. The liquid crystal complexes of
transition metals with giant magnetic anisotropy, spin-crossover properties at room tem-
perature and the magnetic behavior of mesogenic metal-polymers are considered. Espe-
cial attention is devoted to the luminescence properties of lanthanide derivatives.
It is intended for Bachelors in the field of study 18.03.01 «Chemical Technol-
ogy» with the subjects «Physical Chemistry» and «Additional chapters of physical
chemistry», for Masters in the field of study 18.04.01 «Chemical Technology» with the
subjects «Theoretical and experimental research methods in chemistry». The mon-
ograph can be used by PhD students studying in the field of «Chemical Sciences» with
the postgraduate program «Physical Chemistry».
The monograph is prepared at the Department of Physical and Colloidal Chemistry.

UDC 546.443.03
LBC G122-26

ISBN 978-5-7882-2798-6 (ч. II) © Galyametdinov Y., Selivanova N.,
ISBN 978-5-7882-2796-2 Knyazev A., 2020
© Kazan National Research Technological
University, 2020
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CONTENTS

INTRODUCTION ......................................................................................... 5

1.SYNTHESIS AND MESOPHASE IDENTIFICATION

OF D- AND F-ELEMENTS CONTAINING METALLOMESOGENS ...... 6
1.1. Paramagnetic liquid crystalline nickel(II) compounds……...……. 6
1.2. Spectroscopic and thermodynamic properties of Er3+, Nd3+
and Tb3+ containing liquid crystals ......................................................... 10

1.3. Arrangement of trace metal contaminations in thin films
of liquid crystals studied by X-ray standing wave technique .................. 14

1.4. Tris(β-diketonates) lanthanum nematic adducts ........................ 22

2. FERROCENE DERIVATIVES LIQUID CRYSTALS .......................... 31

2.1. Synthesis, computational modelling and liquid crystalline
properties of some [3]ferrocenophane-containing Schiff’s bases
and β-aminovinylketone: Molecular geometry phase behaviour
relationship ............................................................................................. 31

2.2. A Novel Series of Heteropolynuclear Metallomesogens:
Organopalladium Complexes with Ferrocenophane-Containing
Ligands ................................................................................................... 43

3. LYOTROPIC METALLOMESOGENS ................................................. 51

3.1. Mesogenic and Luminescent Properties
of Lyotropic Liquid Crystals Containing Eu(III) and Tb(III) ions .......... 51

3.2. Hybrid silica luminescent materials based on lanthanide-
containing lyotropic liquid crystal with polarized emission .................... 64

3.3. Lyotropic La-containing lamellar liquid crystals:
phase behaviour, thermal and structural properties ................................. 73

3.4. Modification of nonionic vesicles by adding decanol
and functional lanthanide ions ................................................................ 84

3.5. Evaluation of Interactions between Liquid Crystal Films
and Silane Monolayers by Atomic Force Microscopy ............................ 99

3.6. Phase behaviour, structural properties and intermolecular
interactions of systems based on substituted thiacalix [4] arene
and nonionic surfactants ....................................................................... 106

3.7. Lyotropic mesomorphism of rare-earth trisalkylsulphates
in the water-ethylene glycol system ...................................................... 115

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4. LUMINESCENT PROPERTIES OF MESOGENES ........................... 119

4.1. Polarized Luminescence from Aligned Samples
of Nematogenic Lanthanide Complexes ............................................... 119

4.2. Mesomorphic behaviour and luminescent properties
of mesogenic β-diketonate lanthanide adducts
with 5,5′-di(heptadecyl)- 2,2′-bipyridine .............................................. 127

4.3. Ab Initio Study of Energy Transfer Pathways in Dinuclear
Lanthanide Complex of Europium(III) And Terbium(III) Ions ............. 134

4.4. Influence of Structural Anisotropy on Mesogenity
of Eu(III) Adducts and Optical Properties of Vitrified Films Formed
on their Base ......................................................................................... 148
4.5. Changes in luminescent properties of vitrified films
of terbium(III) β-diketonate complex upon UV laser irradiation .......... 158

4.6. Influence of Lewis bases on mesogenic and luminescent
properties of Eu(III) tris(β-diketonates) adducts homogenous films ..... 169

4.7. Influence of Eu(III) Complexes Structural Anisotropy
on Luminescence of Doped Conjugated Polymer Blends ..................... 178

4.8. Controlled polarized luminescence of smectic
lanthanide complexes ........................................................................... 191

4.9. A photostable vitrified film based on a terbium(III)-
diketonate complex as a sensing element for reusable luminescent
thermometers ........................................................................................ 204

4.10. Optical and structural characteristics of PMMA films
doped with a new anisometric Eu(III) complex .................................... 215

4.11. Photostable Anisometric Lanthanide Complexes
as Promising Materials for Optical Applications .................................. 226

CONCLUSION ......................................................................................... 237

REFERENCES .......................................................................................... 238

ABOUT AUTHORS ................................................................................. 290

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INTRODUCTION

Metallomesogens or metal-containing liquid crystals – a class of com-
pounds combining the physical characteristics exhibited by metal coordina-
tion complexes with those of organic molecules which give liquid crystals.
Such compounds were first synthesized over 110 years ago but the topic has
achieved a distinctive character only thirty years ago. Today, the develop-
ment of nanotechnology leads to new areas of metallomesogens application
in biomedicine and diagnostics, optical material designs for electronic and
optoelectronic.
The scope for metallomesogens is great, as there are some 60 metals
which, in principle, can be coordinated to organic ligands. Metals also show a
remarkable variety of geometries and the incorporation of a metal immediately
opens up a wide choice of new geometric shapes. Further important effects
arise from the large and polarizable electron density which is a feature of every
metal atom. Many metal ions of the d- and f-block elements have unpaired
electrons and are colored, their inclusion opens up the capabilities of new
physical properties in liquid crystals. Because mesophase formation depends
on intermolecular forces and the space around the metal is occupied by the
ligand, the liquid crystal properties of metallomesogens are dominated by the
ligands and their arrangement, in other words by the overall shape of the mol-
ecule. Thus, for example, long monodentate ligands (or bidentate ones with
small bite angles) will tend to give rodlike nematics and smectics. The flat,
disklike polydentate ligands (like macrocycles) will give discotics. Specific
physicochemical properties will be determined by a metal ion.
This monograph is devoted to the study of metallomesogens by Rus-
sian group of scientists led by Galyametdinov Y. G. In the first part, covering
the English versions of publications, the results of the synthesis and experi-
mental studies of some theoretical works in the field of magnetism and optics
of metallomesogens were considered. Some results of the practical applica-
tion of metal-containing liquid crystals in promising fields of science and
technology are considered.
Present book presents synthesis and mesophase identification of d- and
f-elements containing metallomesogens. Synthesis, computational modelling
and liquid crystalline properties of some [3]ferrocenophane-containing
Schiff’s bases and β-aminovinylketone are described. Mesogenic and
luminescent properties of lyotropic rare-earth containing system are devoted.
These systems were the base for creation of hybrid silica luminescent material
with polarized emission. Luminescent properties of thermotropic lantha-
nidomesogens and their complexes in polymer matrices are considered.
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1. SYNTHESIS AND MESOPHASE IDENTIFICATION
OF D- AND F-ELEMENTS CONTAINING METALLOMESOGENS

1.1. Paramagnetic liquid crystalline nickel(II) compounds

Copper(II), nickel(II) and oxovanadium(IV) complexes of 4-(4-hep-
tyloxybenzoyloxy)-N-(S)-2-methylbutylsalicylaldimine, as well as the par-
ent ligand, were studied by optical and DSC methods. For the first two com-
plexes, there exist between a tightly twisted chiral nematic phase and the iso-
tropic liquid either some blue phases or novel-type amorphous phases, with
their temperature ranges depending significantly on the metal centre. For the
third complex, direct isotropization takes place.
It is a well known property of liquid crystals that strong disymmetry
of molecules, resulting in their high twisting ability, can generate novel chiral
mesophases [1–2]. Among them there are blue phases, existing between the
chiral nematic (N*) phase and the isotropic liquid [2]. Most probably, a sim-
ilar situation arises also in systems having a twist-grain-boundary smectic
A* phase [3]. Recently, an intermediate phase (IP) formed by paramagnetic
copper metallomesogens was reported and tentatively identified as a blue
phase [4]. In this communication we confirm the existence of such paramag-
netic IPs and compare their properties for different chelated metal ions.
Since complexation of a divalent transition metal ion by bidentate chi-
ral ligands doubles the number of chiral centres within the resulting complex
molecules, the twisting power of such complexes should become much
higher than that of the parent ligand, and the helical pitch much tighter.
The helical pitch is a major factor which controls the presence and tempera-
ture range of particular blue phases [5, 6]. For complexes, therefore, we ex-
pect an enhanced stability of these phases.
Complexes 7ML (fig. 1.1), as well as their parent ligand,
2
7HL = 4-(4-heptyloxybenzoyloxy)-N-(S)-2 methylbutylsalicylaldimine,
were chosen for our studies. Their syntheses were performed simi-
larly to those reported in [7]. As a chiral substrate we used
S(–)-2-methylbutylamine, [α] 20-5,9°, obtained from Aldrich. Synthetic de-
D
tails, analytical data and magnetic properties will be described elsewhere.
Besides an obvious paramagnetism for the copper and oxovanadium com-
plexes, a weak paramagnetism is observed for the nickel analogue (cf. [7] for
properties of some related compounds).

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Fig. 1.1. Chemical structure of investigated compounds nML ,
2
where M = Cu, Ni, Vo, Pd

All compounds, when studied microscopically, reveal the presence of
a chiral nematic phase; no other mesophases were detected. For the ligand, a
selective light reflection was observed, and so a helical pitch of 0,3–
0,4 pm, in the temperature range 50–40 °C, was estimated. For the com-
plexes, selective light reflection was observed only for samples diluted by
achiral metallo-mesogens or conventional nematics, which proves that the
pure chiral complexes are rather tightly twisted. Their helix was found to be
right-handed by applying the contact method, using cholesteryl chloride
(RH) and propionate (LH) as standards. Such handedness is in agreement
with the empirical SED rule [8].
Since a high twist can generate blue phases with a short lattice con-
stant, the question arises as to whether such phases are present in the com-
plexes under study. Our approaches to detecting them by means of obser-
vation of selective light reflection or a transmission dip in the UV spectra
have failed. On the other hand, the strong optical absorption of the samples,
and not the absence of these phases, might be the decisive factor here.
To elucidate the situation, we used differential scanning calorimetry (DSC).
This method, if carefully applied, sometimes detects blue phases unobserva-
ble in the visible range [9].
Using a Perkin-Elmer DSC-7 and optimizing all the experimental pa-
rameters involved, we obtained good quality thermograms for all the com-
pounds. For the ligand, above its melting temperature, a typical
A-shaped isotropization peak is observed, confirming the lack of blue phases.
The thermograms of the complexes are distinctly different (fig. 1.2).
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Fig. 1.2. DSC curves for 4-(4-heptyloxybenzoyloxy)-N-(S)-
-2-methylbutylsalicylaldimine complexes: а – 7CuL (sample 6,1 mg, scan
2
1 °C min-1); b – 7NiL (6,1 mg, 1 °C min-1); c – 7VOL (4,9 mg, 2 °C min-1)
2 2

The most simple occurs in the case of 7VOL , for which only a signal
2
for a phase transition to an isotropic liquid is present. However, the ab-
sence of pre-transitional anomalies in the specific heat, as well as an ex-
tremely low enthalpy change for the phase transition, should be noticed.
The corresponding entropy change is only 0.095 R. Such behaviour would
correspond, in terms of the Landau-de Gennes model, to a small value of the
pre-transitional coefficient, a, in the free energy expansion for the system.
There is also a simple interpretation of the DSC data for 7NiL , for which the
2
thermogram corresponds fully to the response of a system having a chiral ne-
matic phase and blue phases. Two small peaks corresponditig to transitions
relating to intermediate phases are overlapped on one side of the isotropization
peak. Furthermore, typical for blue phases are the temperature ranges of the
phases (0–28 °C and 0–81 °C) and the transition enthalpies (table 1.1).

Table 1.1
Phase transition temperatures (°C) and, inparentheses, enthalpies
(J·g–1) for the ligand, 7HL = 4-(4-heptgloxybenzoyloxy)-N-(S)-
2-methylbutylsalicylaldimine, and its Cu(II), Ni(II)
and VO(IV) complexes

Phases: C, crystal; N, nematic; I, isotropic liquid; IP, intermediate phase; ●, the phase exists; –, the phase does not exist.
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In contrast to these complexes, for the copper anaiogue, some non-
typical, but nevertheless reproducible, thermograms were recorded. The iso-
tropization peak is diffuse over a broad temperature range. This broadening
is more likely to result from specific heat pre-transitional anomalies and is
certainly not connected with contamination of the samples. The thermograms
were confirmed for samples synthesized independently in two laboratories
and they do not change after subsequent recrystallizations. Moreover, the low
temperature peak, corresponding to the N*-IP transition, is very sharp. This
phase transition is obviously first order (a small hysteresis in the phase tran-
sition temperature is also observed) with an unexpectedly high transitional
enthalpy and no pre-transitional effects. In general, the thermogram is, toutes
proportions gardtes, similar to those observed for some smectic A* systems
with an amorphous phase of unknown structure [3].
Although the presence of the BP(III) alone is expected for short
pitched chiral nematogens [10], the existing experimental data do not suf-
fice to prove that the intermediate, 2,7 °C wide, mesophase of 7CuL is
2
this blue phase. Besides optical studies (difficult to perform with an inher-
ent light absorption), phase diagram studies also appeared unrealistic.
Construction of detailed binary phase diagrams, with reference sub-
stances, was too subtle a task, bearing in mind both the narrow tempera-
ture range involved and the low enthalpy of the N*-BP(III) transition for
the standards. The intermediate phase, because of its unusual thermal
properties, might even be an entirely novel phase which exhibits a near-
continuous phase transition to an isotropic liquid. To study the molecular
organization of the phase, NMR analysis is inappropriate because of its
paramagnetic properties. EPR studies could be more promising; this
method has proved to be applicable to some chiral systems.
A tentative DSC examination of the diamagnetic analogues, 12NiL
2
and 12PdL also reveals the presence of intermediate phases. In addition, the
2
phase for the Palladium(II)-complex is detectable optically; it appears as
a fog-like texture.
In comparing the thermal stabilities of the complexes, we find that both
the isotropization temperatures and the enthalpies are ranged in the sequence
NIL > CuL > VOL . We checked that this sequence holds for Shiff’s base
2 2 2
complexes having normal as well as α- and β-branched N-alkyl substituents.
This fact points to the role of the metal centre as a factor determining molec-
ular shape (through the coordination geometry) and molecular interactions.
In contrast, it is difficult to explain why the temperature range of the interme-
diate phases is wider for CuL than for NIL . Phase transitions in chiral
2 2
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systems are determined by the chirality, k = q (K a/b2)1/2 (2a)], rather
o 1
than simpiy by the inverse helical pitch, p–1 = q /2π. As yet, not much is
0 0
known about the additional elastic (K) and free energy (a, b) constants for
complexes. However, in view of our DSC results, a relatively low chirality,
resulting from a small value of the a factor, might be responsible for the ab-
sence of any intermediate phases for the 7VOL compound. This effect might
2
be connected with the marked non-planarity of oxovanadium complexes.
To summarize, for these metal complexes specified and having two
chiral centres, mesophases intermediate between the nematic and isotropic
liquids exist, in contrast to the parent, chiral ligand. The role of the metal
centre, which influences the occurrence, temperature range and type of these
phases, is not clear at present.

1.2. Spectroscopic and thermodynamic properties of Er3+, Nd3+
and Tb3+ containing liquid crystals

A ligand and three metallo-organic complexes containing Nd3+, Th3+
and Er3+ ions were synthesized. Absorption, linear dichroism spectroscopy
and domain structures investigations plus X-ray difractometry measurements
at heating-cooling cycles were performed. An influence of a rare earth metals
on LC thermodynamic properties have been discussed.
Metal-containing liquid ciystals have been known for long time since
Vorländer in 1910 discovered thermotropic phase in alkali metal carbox-
ylates. Nevertheless, only after an publication of an pioneer work on
mesogemc nickel and platinum complexes by Giroud-Godquin and Muller-
Westenhoff in l977 an interest to such materials grew up. These new liquid
crystal materials were intensively investigated during last decade. Mostly
they are aromatic compounds containing heteroatoms, which are able to bind
metals and create stable metal complexes as liquid ciystals. In broad terms
this means that the dipole-dipole and dispersion forces which hold LC in an-
isotropic supramolecular arrays, are not destroyed by an introduction of the
metal ions. Indeed, in some cases the mesophases found are identical to those
exhibited by the organic ligands themselves [11, 12]. The aim of this work is
to establish a contribution of rare-earth ions to macroscopic properties of LC.
A ligand and three metallo-organic complexes containing Nd3+, Tb3+
and Er3+ ions were synthesized.
Absorption, linear dichroism spectroscopy in visible region and
X-ray diffractometry measurements were performed plus microscopic inves-
tigation of the domain structures in heating-cooling cycles. Linear dichroism
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