smiles create 5 different molecular SMILE's for possible stable hybrid "Diamond Cadmium Telluride Lattice" molecule. Attach a ring of [Cd+2].[TeH2-] and Ferrocene molecules around all the inner rings free connections.

ferro diamond .txt

Write valid molecular SMILE for [Cd]=[Te]  bonded to  λ²-iron(2+) bis(cyclopenta-2,4-dien-1-ide) 

[Cd]=[Te]-c1cc([Fe])c([Fe])c1




Noise:

CC([TeH2-])=CC([TeH2-])
CC([TeH2-])=CC1([TeH2-])CCCC1([TeH2-])
CC([TeH2-])=CC1([TeH2-])CC([TeH2-])CC1([TeH2-])
CC([TeH2-])=CC1([TeH2-])CC([TeH2-])CC([TeH2-])CC1([TeH2-])
CC([TeH2-])=CC1([TeH2-])CC([TeH2-])CC([TeH2-])CC([TeH2-])CC1([TeH2-])

Cd[TeH2]1.F[C@@H]2C=CC=CC2.F[C@@H]2C=CC=CC2.F[C@@H]2C=CC=CC2.F[C@@H]2C=CC=CC2.F[C@@H]2C=CC=CC2

Cd[TeH2]1.F[C@@H](C=C)C.F[C@@H](C=C)C.F[C@@H](C=C)C.F[C@@H](C=C)C.F[C@@H](C=C)C

Cd[TeH2]1.F[C@H](C#N)C.F[C@H](C#N)C.F[C@H](C#N)C.F[C@H](C#N)C.F[C@H](C#N)C

Cd[TeH2]1.F[C@H](C(=O)[O-])C.F[C@H](C(=O)[O-])C.F[C@H](C(=O)[O-])C.F[C@H](C(=O)[O-])C.F[C@H](C(=O)[O-])C

Cd[TeH2]1.F[C@H](Cl)C.F[C@H](Cl)C.F[C@H](Cl)C.F[C@H](Cl)C.F[C@H](Cl)C

Cd[TeH2]1.F[C@@H](C=C)C.F[C@@H](C=C)C.F[C@@H](C=C)C.F[C@@H](C=C)C.F[C@@H](C=C)C
Cd[TeH2]1.F[C@H](C#N)C.F[C@H](C#N)C.F[C@H](C#N)C.F[C@H](C#N)C.F[C@H](C#N)C
Cd[TeH2]1.F[C@H](C(=O)[O-])C.F[C@H](C(=O)[O-])C.F[C@H](C(=O)[O-])C.F[C@H](C(=O)[O-])C.F[C@H](C(=O)[O-])C
Cd[TeH2]1.F[C@H](Cl)C.F[C@H](Cl)C.F[C@H](Cl)C.F[C@H](Cl)C.F[C@H](Cl)C