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New
Series
Numerical Data
and Functional Relationships
in Science and Technology
GROUP II VOLUME 31
Molecules
and
Radicals
Magnetic
Properties of
Paramagnetic
Compounds
SUBVOLUME C
Part 3
MATERIALS.SPRINGER.COM
123
Landolt-Bo€rnstein: Numerical Data and Functional
Relationships in Science and Technology – New Series
Volume 31C
Landolt-B€ornstein
Numerical Data and Functional Relationships
in Science and Technology
New Series
Geophysics (Group V)
Some of the group names have been changed to provide a better description of their contents.
A. Gupta
Editor
Magnetic Properties of
Paramagnetic Compounds
Subvolume C
R. T. Pardasani, P. Pardasani
Authors
Editor
A. Gupta
Department of Chemistry
University of Delhi
Delhi, India
Authors
R. T. Pardasani P. Pardasani
Department of Chemistry Department of Chemistry
School of Chemical Sciences and University of Rajasthan
Pharmacy, Central University of Jaipur, India
Rajasthan
Bandar Sindri, Ajmer, India
In continuation to our efforts to update the magnetic susceptibility data of paramagnetic compounds, a new
Volume II/31C is presented herewith covering literature partly from 1991 to 1995. Since most of the
researchers these days consult the literature online, a new pattern is being introduced with effect from this
volume. All the magnetic properties of each individual substance are listed as a single document which is
self-explainable and allowing search in respect of substance name, synonyms, common vocabulary, and
even structure. It is hoped that a new pattern will facilitate greater accessibility of magnetic data and
enhance the use of Landolt-B€ornstein.
The editor wishes to express her thanks to the authors R. T. Pardasani and Pushpa Pardasani for this
excellent volume. The encouraging support of Dr. Wolfgang Finger from Springer is gratefully acknowl-
edged.
v
Contents
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1
Magnetic properties of di-μ-hydroxo-bis(bipyridyl)dicopper(II) sulphate pentahydrate . . . . . 11
Magnetic properties of bis{copper(II)} complex of ascidiacyclamide . . . . . . . . . . . . . . . . . . . . 13
Magnetic properties of dafone chlorocuprate complex . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 15
Magnetic properties of a mixed valence copper (I, II) phosphate . . . . . . . . . . . . . . . . . . . . . . . 17
Magnetic properties of copper(II) porphyrin п-cation radical . . . . . . . . . . . . . . . . . . . . . . . . . 19
Magnetic properties of di-μ-hydroxo-bis(1, 10-phenanthroline)dicopper(II) sulphate
pentahydrate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 21
Magnetic properties of di-μ-hydroxo-bis(N, N, N0 , N0 -tetramethylethylenediamine)
dicopper(II) nitrate trihydrate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 23
Magnetic properties of dinuclear copper(II) complex of Schiff base derived from 2,
6-diformyl-4-methylphenol and 1-aminoethane . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 25
Magnetic properties of polymeric, two dimensional μ, 2, 20 -bipyrimidine, μ-oxalato
bridged and μ-chloro-bridged copper(II) complex . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 27
0
Magnetic properties of copper(II) complex of N, N -bis(2-cyanoethyl)-5, 7-dioxo-1, 4, 8,
11-tetraazacyclotetradecane . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 29
Magnetic properties of π-cation radical of Cu(II) porphyrin . . . . . . . . . . . . . . . . . . . . . . . . . . 31
Magnetic properties of dinuclear copper(II) complex of Schiff base derived from 2,
6-diformyl-4-methylphenol and 1, 2-diaminoethane . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 33
Magnetic properties of dinuclear copper(II) complex of Schiff base derived from 2,
6-diformyl-4-methylphenol and 1, 3-diaminopropane . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 35
Magnetic properties of copper(II) methylphosphonate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 37
Magnetic properties of copper(II) ethylphosphonate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 40
Magnetic properties of copper(II) phenylphosphonate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 42
Magnetic properties of α-copper(II) methylphosphonate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 45
Magnetic properties of α-copper(II) ethylphosphonate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 47
Magnetic properties of α-copper(II) phenylphosphonate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 49
Magnetic properties of β-copper(II) methylphosphonate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 51
Magnetic properties of trimetallic(Cu3) oxomethylphosphonate dehydrate . . . . . . . . . . . . . . . 53
Magnetic properties of Bis[(μ-nitrato-O)bis(nitrato)bis(μ-pyridazine)(pyridazine)
copper(II)]copper(II) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 55
Magnetic properties of (nitrato)(nitrato-O, O’)tris(pyridazine)copper(II) . . . . . . . . . . . . . . . . 57
Magnetic properties of bis(nitrato)tetrakis(pyridazine)copper(II) . . . . . . . . . . . . . . . . . . . . . . 59
vii
viii Contents
Magnetic properties of tetravalent niobium phenyl stabilized by anionic organic amides . . . . 869
Magnetic properties of tetravalent niobium methyl stabilized by anionic organic amides . . . . 871
Magnetic properties of tetravalent niobium enolate stabilized by anionic organic amides . . . . 873
Magnetic properties of 3-indole carboxylate complex of niobocene dichloride . . . . . . . . . . . . . 875
Magnetic properties of mononuclear tantalum(0) carbonyl compound . . . . . . . . . . . . . . . . . . 877
Magnetic properties of monomeric chromium(II) aryl . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 879
Magnetic properties of monomeric pyridine adduct of chromium(II) aryl . . . . . . . . . . . . . . . . 881
Magnetic properties of dimeric chromium(II) aryl . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 883
Magnetic properties of monomeric chromium(III) aryl . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 885
Magnetic properties of monomeric chromium(III) aryl . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 887
Magnetic properties of polycyclophosphane complex of cyclopentadienyl chromium(I) . . . . . . 889
Magnetic properties of heteronuclear sulfide bridged chromium and rhenium containing
cluster (cis-isomer) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 890
Magnetic properties of heteronuclear sulfide bridged chromium and rhenium containing
cluster (trans-isomer) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 892
Magnetic Properties of Tetranuclear Sulfide Bridged Chromium and Rhenium Cluster
Containing Carbonyl and Nitrosyl Ligands . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 894
Magnetic properties of triangular sulfide bridged chromium and rhenium cluster
containing carbonyl and nitrosyl ligands . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 896
Magnetic properties of tetranuclear sulfide bridged chromium and rhenium cluster
containing carbonyl ligand . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 898
Magnetic properties of triangular sulfide and oxothiolate bridged chromium and
rhenium cluster containing chloro, carbonyl and nitrosyl ligands . . . . . . . . . . . . . . . . . . . . . . 900
Magnetic properties of sulfide and thiolate bridged triangular cluster with CrRe2 core
containing carbonyl and nitrosyl ligands . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 902
Magnetic properties of sulfide and thiolate bridged triangular cluster with CrRe2 core
containing carbonyl and nitrosyl ligands . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 904
Magnetic properties of sulfide and thiolate bridged antiferromagnetic cluster with Cr2Re
core containing carbonyl and nitrosyl ligands . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 906
Magnetic properties of fac(S)-tris(2-aminoethanethiolato) chromium(III) . . . . . . . . . . . . . . . . 908
Magnetic properties of S-bridged zinc bromide polynuclear complex composed of
fac-(S)-[Cr(aet)3] units . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 909
Magnetic properties of S-bridged nickel bromide polynuclear complex composed of
fac-(S)-[Cr(aet)3] units . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 911
Magnetic properties of S-bridged zinc nitrate polynuclear complex composed of
fac-(S)-[Cr(aet)3] units . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 914
Magnetic properties of S-bridged nickel nitrate polynuclear complex composed of
fac-(S)-[Cr(aet)3] units . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 915
Magnetic properties of imidodiphosphinoselenido complex of chromium(III) . . . . . . . . . . . . . 916
Contents xxv
Some of the species of the old genus Eremiaphila (Fig. 144) are of
very unusual form. De Saussure considers that some species of this
genus are more highly modified than any other animals for
maintaining their existence in desert regions. They are said to be
found in places where no vegetation exists, and to assimilate in
appearance with the sandy soil, the species varying in colour, so that
the individuals agree in tint with the soil on which they dwell. These
Insects are referred to the group Orthoderides, and have a short
prothorax, the alar organs being unsuited for flight. What they live on
is not actually known; although other Insects are the natural food of
Mantids, it is said that these desert-frequenting species occur in
spots where no other Insect life is known to exist. Lefebvre[181] met
with these Eremiaphilas in the desert between the Nile and the
Northern Oasis, El Bahryeh, but was quite unable to discover their
mode of subsistence. These Insects are very rare in collections, and
the information we possess about them is very meagre.
"These Insects all came from the same locality, having been
forwarded to Mr. Buckland by Mr. Larymore of the Central Jail at
Midnapur. Mr. Larymore had procured them from the neighbouring
country district, where Santál women and children had hunted them
out and brought them in, hanging on branches or twigs of a bush,
somewhat like a wild plum-tree. They are also said to be found upon
rose-bushes, and in connexion with this it was observed that, in
Midnapur, they were known as rose-leaf Insects, from the
circumstance that when the Insect is more developed and furnished
with wings, the foliaceous appendages are said greatly to increase in
size, and exactly to resemble rose-leaves. Dr. Anderson, however,
was disposed to think that more than one species might probably
occur in the Midnapur district, and that these Insects with the larger
foliaceous expansions might be distinct from the species now before
the Society.
Fig. 146.—Gongylus gongylodes, female. East India.
"Mr. Buckland had made over these Insects to Dr. Anderson, and
since that time they have been regularly fed upon house-flies and
grasshoppers; the latter, however, appear to be rather too strong for
them, and they therefore prefer the flies. They have been tried with
small fragments of plaintain and custard-apple, which they not only
eat, but the juice of which they seem to suck with considerable
avidity, Dr. Anderson, however, thought that it was the moisture of
these fruits that was the chief attraction to these Insects, for the
entire character of their organisation indicated a raptorial habit.
"The reason which induced Dr. Anderson to bring them to the notice
of the Society had now to be pointed out. On looking at the Insects
from above, they did not exhibit any very striking features beyond the
leaf-like expansion of the prothorax and the foliaceous appendages
to the limbs, both of which, like the upper surface of the Insect, are
coloured green, but on turning to the under surface the aspect is
entirely different. The leaf-like expansion of the prothorax; instead of
being green, is a clear, pale lavender-violet, with a faint pink bloom
along the edges of the leaf, so that this portion of the Insect has the
exact appearance of the corolla of a plant, a floral simulation which is
perfected by the presence of a dark, blackish brown spot in the
centre, over the prothorax, and which mimics the opening to the tube
of a corolla. A favourite position of this Insect is to hang head
downwards among a mass of green foliage, and, when it does so, it
generally remains almost motionless, but, at intervals, evinces a
swaying movement as of a flower touched by a gentle breeze; and
while in this attitude, with its fore-limbs banded violet and black, and
drawn up in front of the centre of the corolla, the simulation of a
papilionaceous flower is complete. The object of the bright colouring
of the under surface of the prothoracic expansion is evident, its
purpose being to act as a decoy to Insects, which, mistaking it for a
corolla, fly directly into the expectant, serrated, sabre-like, raptorial
arms of the simulator. It is no new fact that many Insects resemble
the leaves of plants and trees, and that they manifest forms and
colours which serve to protect them in the struggle for existence, but
so far as Dr. Anderson had ascertained, this was the first recorded
instance of an Insect simulating the corolla of a flower for the evident
purpose of attracting Insects towards it for its sustenance. It is even
more remarkable than this, for it is a localised adaptation for such a
purpose, a portion of the Insect being so modified in form and colour
that the appearance of the corolla of a plant is produced, in
conjunction with the remainder of the long attenuated prothorax,
which at a distance resembles the flower stem; the anterior limbs
when in repose even adding to and heightening the deception."
There are probably about 600 species of Mantidae known; they are
distributed over all the warmer parts of the earth, but there are none
in the cooler regions. Europe possesses some twelve or fourteen
species, most of them confined to the Mediterranean sub-region; a
single species, Mantis religiosa, is frequently found in Central
France, and has been recorded as occurring as far north as Havre.
Although no species is a native of Britain, it is not difficult to keep
them alive here. Denny records[186] that an egg-case of a Mantis
was sent from Australia to England, and that the hatching of the
eggs was completed after its arrival. The young fed readily on flies,
and we are informed that in the neighbourhood of Melbourne, where
this Mantis is plentiful, specimens are placed by the citizens on the
window-blinds of their houses, so that the rooms may be cleared
from flies by means of the indefatigable voracity of the Mantis.
1. Anterior tibiae with the outer edge unarmed beneath or only furnished with
very minute tubercles. (Pronotum not longer than the anterior coxae.)
Tribe 1. Amorphoscelides. (Fig. 141, Mantoidea luteola.)
1′. Anterior tibiae with the outer edge spinose beneath.
2. Anterior femora having the inner edge armed beneath with equal
spines, or with spines in which only the alternate are smaller.
Antennae of the male simple, rarely unipectinate.
3. Tibiae and also the intermediate and hind femora even above.
4. Legs and body with no lobe-like processes. (Antennae simple in
each sex.)
5. Pronotum not forming any dilatation above the insertion of the
coxae, its lateral margins straight or (in the genus Choeradodis)
strongly dilated with the anterior margin not rounded. Tribe 2.
Orthoderides. (Fig. 142, Pyrgomantis; Fig. 143, Choeradodis;
Fig. 144, Eremiaphila turcica.)
5′. Pronotum dilated above the insertion of the coxae, there with the
lateral margins broadened in a round manner, the anterior
margin rounded. Tribe 3. Mantides. (Fig. 140, Iris oratoria.)
4′. Legs or body furnished with lobes. (Posterior femora or segments
of the body with lobes, or vertex of the head conically prolonged.)
Tribe 4. Harpagides. (Fig. 136, Harpax variegatus; Fig. 135,
Deroplatys sarawaca.)
3′. Tibiae as well as the intermediate and hind femora carinate above.
(Pronotum elongate, with the posterior part, behind the transverse
groove, three times as long as the anterior part.) Tribe 5. Vatides.
(Fig. 147, Stenophylla cornigera.)
2′. Anterior femora beneath, with the inner edge armed between the longer
teeth with shorter teeth, usually three in number. Antennae of the
male bipectinate. (Vertex conically prolonged.) Tribe 6. Empusides.
(Fig. 146, Gongylus gongylodes.)
CHAPTER XI
ORTHOPTERA CONTINUED—PHASMIDAE—WALKING-LEAVES—STICK-
INSECTS
These Insects are amongst the most curious of natural objects. They
are frequently of large size, some attaining 9 inches in length (Fig.
162, Palophus centaurus, one-half natural length). Their variety of
form could scarcely be surpassed; their resemblance to products of
the vegetable kingdom is frequently very great: some of the more
linear species (Fig. 148, Lonchodes nematodes) look like sticks or
stems of grass; some have a moss-like appearance, while others
resemble pieces of lichen-covered bark. The members of the tribe
Phylliides are leaf-like. A certain number of other Phasmids are
covered with strong spines, like thorns (Fig. 149). The plant-like
appearance is greatest in the female sex. When there is a difference
between the two sexes as to the organs of flight, these are more fully
developed in the male.
When the young Insect is in the egg, ready for emergence, the
meso- and meta-thorax are not remarkably elongate, so that the
femora are not very far apart, but by the time the creature has fairly
emerged from the prison of its embryonic life the thoracic segments
have attained their usual proportions; much expansion of the body
takes place as the Insect leaves the egg, so that it appears a marvel
how it could have been contained therein; this expansion affects the
parts of the body unequally.
We have pointed out that the tegmina or upper wings are usually of
small size or absent (Fig. 150, Aschipasma catadromus), even in the
species where the lower wings are very largely developed; in such
cases the latter organs are folded in a complicated, fan-like manner,
and repose on the back, looking as if they were really the tegmina
(Fig. 159, Calvisia atrosignata); this appearance, moreover, is in
some species enhanced much by the fact that the part of the wing
which is outermost in the folded state is quite differently coloured
from the rest of the organ. The colour of the body in many
Phasmidae is said to be very variable, and if the tints be owing to
chlorophyll or other plant juices, finding their way amongst the
Insect-tissues, this is readily understood; in Diapheromera the young
Insect is brownish on hatching, becomes green after feeding, and
turns brown again when the leaves do so. The ocelli, too, are said to
be very variable, and M‘Coy goes so far as to state[194] that they
may be either present or absent in different individuals though of the
same species and sex,—a statement so remarkable as to require
minute examination, though it is to some extent confirmed by the
remarks of other entomologists.
Fig. 154.—Phyllium scythe, female. Sylhet. (After Westwood.)